Allele Registry

Canonical Allele Identifier: PA2826709493

Gene: CNGB1 HGNC NCBI

ClinVar RCV:

RCV000364070

RCV001358311

RCV002522880

RCV003922352

ClinVar Variation:

320058

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