Allele Registry

Canonical Allele Identifier: PA645433456

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000277134

RCV000332145

RCV001239882

ClinVar Variation:

363868

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Pro750Ser	CA4799764 NM_019098.5:c.2248C>T