Canonical Allele Identifier: PA645480670
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_001288.3:p.Ala1141Thr
CA8082571
NM_001297.5:c.3421G>A