Canonical Allele Identifier: PA2826709046
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320078
ClinVar RCV Id: RCV000288196 RCV001458432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Leu812Ile
CA8083004
NM_001286130.2:c.2434C>A