Allele Registry

Canonical Allele Identifier: PA202719

Gene: CRX HGNC NCBI

ClinVar RCV:

RCV000086004

RCV000178122

RCV000308806

RCV000347317

RCV000390414

RCV001081848

RCV002498461

ClinVar Variation:

99608

HGVS (amino-acid)	Matching Registered Transcripts
NP_000545.1:p.Ala158Thr	CA202718 NM_000554.6:c.472G>A