Allele Registry

Canonical Allele Identifier: PA269687

Gene: RB1 HGNC NCBI

ClinVar Allele:

132304

ClinVar RCV:

RCV000114686

ClinVar Variation:

126794

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Asp701Asn	CA026421 NM_000321.3:c.2101G>A