Allele Registry

Canonical Allele Identifier: PA645480668

Gene: CNGB1 HGNC NCBI

ClinVar Variation Id: 320063

HGVS (amino-acid)	Matching Registered Transcripts
NP_001288.3:p.Ala1114Thr	CA8082590 NM_001297.5:c.3340G>A