Canonical Allele Identifier: PA2826709131
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_001273059.1:p.Gly862Asp
CA8082916
NM_001286130.2:c.2585G>A