Allele Registry

Canonical Allele Identifier: PA645433330

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000301489

RCV000356262

RCV000931567

RCV001276129

ClinVar Variation:

363872

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Ala511Thr	CA4799987 NM_019098.5:c.1531G>A