Allele Registry

Canonical Allele Identifier: PA113650

Gene: RB1 HGNC NCBI

ClinVar RCV:

RCV000013947

ClinVar Variation:

13072

HGVS (amino-acid)	Matching Registered Transcripts
NP_000312.2:p.Ser567Leu	CA026396 NM_000321.3:c.1700C>T