Allele Registry

Canonical Allele Identifier: PA645433463

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000261883

RCV000356702

RCV001034257

ClinVar Variation:

363867

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Val770Phe	CA4799753 NM_019098.5:c.2308G>T