Allele Registry

Canonical Allele Identifier: PA229001

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000087167

RCV001854506

ClinVar Variation:

100809

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Leu665Arg	CA026418 NM_000321.3:c.1994T>G