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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRKCH, PRKCH-AS1
(K65R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PRKCH, PRKCH-AS1
(R110C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
PRKCH, PRKCH-AS1
(G55A)
Single nucleotide variant
(missense variant)
Ischemic stroke
GUncertain significance
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