Canonical Allele Identifier: PA645480485
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 281324
ClinVar RCV Id: RCV000285588 RCV000340906 RCV001521801
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288.3:p.Ala527Val
CA8083387
NM_001297.5:c.1580C>T