Allele Registry

Canonical Allele Identifier: PA2826380827

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000260491

RCV001711958

ClinVar Variation:

337965

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243200.1:p.Arg131Ser	CA9793672 NM_001256271.2:c.391C>A