Canonical Allele Identifier: PA2826709407
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320063
ClinVar RCV Id: RCV000380180 RCV001519492 RCV003888753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Ala1108Thr
CA8082590
NM_001286130.2:c.3322G>A