Canonical Allele Identifier: PA2826709447
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320060
ClinVar RCV Id: RCV000376862 RCV001092933 RCV003888751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Ala1135Thr
CA8082571
NM_001286130.2:c.3403G>A