Canonical Allele Identifier: PA2826709493
Gene: CNGB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 320058
ClinVar RCV Id: RCV000364070 RCV001358311 RCV002522880 RCV003922352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273059.1:p.Arg1181Gln
CA8082505
NM_001286130.2:c.3542G>A