Canonical Allele Identifier: PA229001
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 100809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Leu665Arg
CA026418
NM_000321.3:c.1994T>G