Allele Registry

Canonical Allele Identifier: PA228999

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000087166

RCV001854505

ClinVar Variation:

100808

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Val654Met	CA026413 NM_000321.3:c.1960G>A