Allele Registry

Canonical Allele Identifier: PA2826380899

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000005561

RCV001140685

ClinVar Variation:

5249

HGVS (amino-acid)	Matching Registered Transcripts
NP_001243201.1:p.Leu159Met	CA117357 NM_001256272.2:c.475T>A