Allele Registry

Canonical Allele Identifier: PA215759

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000034597

RCV000492290

RCV000601517

RCV001079302

ClinVar Variation:

41685

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Asp210Tyr	CA026464 NM_000321.3:c.628G>T