Canonical Allele Identifier: PA645480543
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320085
ClinVar RCV Id: RCV000263840 RCV002056505
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288.3:p.Glu624Gln
CA8083252
NM_001297.5:c.1870G>C