Canonical Allele Identifier: PA2826708684
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320091
ClinVar RCV Id: RCV000328036 RCV000597493 RCV001075314
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Pro538Leu
CA8083377
NM_001286130.2:c.1613C>T