Allele Registry

Canonical Allele Identifier: PA113476

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV001899288

ClinVar Variation:

1370241

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Arg358Gly	CA388161148 NM_000321.3:c.1072C>G