Allele Registry

Canonical Allele Identifier: PA161796

Gene: RB1 HGNC NCBI

ClinVar Allele:

138859

ClinVar RCV:

RCV000121920

RCV000457901

RCV000572000

RCV001570931

RCV003905163

ClinVar Variation:

135120

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Arg621Ser	CA026403 NM_000321.3:c.1861C>A