Allele Registry

Canonical Allele Identifier: PA645432948

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000277976

RCV000325972

RCV000900243

RCV001272756

ClinVar Variation:

363888

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Gly15Arg	CA4800544 NM_019098.5:c.43G>C CA371452853 NM_019098.5:c.43G>A