Allele Registry

Canonical Allele Identifier: PA227613

Gene: CRX HGNC NCBI

ClinVar Allele:

105485

ClinVar RCV:

RCV000085991

RCV001369855

ClinVar Variation:

99596

HGVS (amino-acid)	Matching Registered Transcripts
NP_000545.1:p.Ala56Thr	CA227612 NM_000554.6:c.166G>A