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Links from Gene

Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRT12
(D175N)
Single nucleotide variant
(missense variant)
Corneal dystrophy, Meesmann, 1
GBenign
KRT12
(E330*)
Single nucleotide variant
(nonsense)
Corneal dystrophy, Meesmann, 1
GUncertain significance
KRT12
(R19W)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(V143L)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(A137P)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(R135S)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(Q130P)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(L433R)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(R430P)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(Y429C)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(I426S)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
(I426V)
Single nucleotide variant
(missense variant)
not provided
Gnot provided
KRT12
Single nucleotide variant
not provided
Gnot provided
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