U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Links from Gene

Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRXL2B, MMEL1
(A759T)
Single nucleotide variant
(3 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
MMEL1, PRXL2B
(R766W)
Single nucleotide variant
(3 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
MMEL1, PRXL2B
(H763R)
Single nucleotide variant
(3 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
MMEL1, PRXL2B
(H771Y)
Single nucleotide variant
(3 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
Format
Sort by
Choose Destination