Allele Registry

Canonical Allele Identifier: PA117356

Gene: VSX1 HGNC NCBI

ClinVar RCV:

RCV000005560

RCV000358879

RCV000454465

RCV002054416

ClinVar Variation:

5248

HGVS (amino-acid)	Matching Registered Transcripts
NP_055403.2:p.Gly160Asp	CA117355 NM_014588.6:c.479G>A