Allele Registry

Canonical Allele Identifier: PA645433211

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000242961

RCV000286399

RCV000376272

RCV001272487

RCV001510548

ClinVar Variation:

261092

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Ile307Val	CA4800218 NM_019098.5:c.919A>G