Allele Registry

Canonical Allele Identifier: PA916062859

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000260491

RCV001711958

ClinVar Variation:

337965

HGVS (amino-acid)	Matching Registered Transcripts
NP_955457.1:p.Arg131Ser	CA9793672 NM_199425.3:c.391C>A