Canonical Allele Identifier: PA658747023
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 493184
ClinVar RCV Id: RCV000585175 RCV001119757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001288.3:p.Gly868Asp
CA8082916
NM_001297.5:c.2603G>A