Allele Registry

Canonical Allele Identifier: PA645433335

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000336568

RCV000394987

RCV000487572

RCV001700999

RCV001833481

ClinVar Variation:

363871

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Ile512Val	CA4799986 NM_019098.5:c.1534A>G