Canonical Allele Identifier: PA227613
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 99596
ClinVar RCV Id: RCV000085991 RCV001369855
JSON-LD

Amino-acid Alleles

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