Allele Registry

Canonical Allele Identifier: PA891845819

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000709347

ClinVar Variation:

584871

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Arg467Gly	CA388162691 NM_000321.3:c.1399C>G