Allele Registry

Canonical Allele Identifier: PA645433142

Gene: CNGB3 HGNC NCBI

ClinVar RCV:

RCV000250693

RCV000364988

RCV000988079

RCV001522473

RCV001833281

ClinVar Variation:

261090

HGVS (amino-acid)	Matching Registered Transcripts
NP_061971.3:p.Cys234Trp	CA4800300 NM_019098.5:c.702T>G