Allele Registry

Canonical Allele Identifier: PA916062847

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000005563

RCV000396085

RCV003934801

ClinVar Variation:

5251

HGVS (amino-acid)	Matching Registered Transcripts
NP_955457.1:p.Leu17Pro	CA117359 NM_199425.3:c.50T>C