Canonical Allele Identifier: PA161794
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135119

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala525Thr
CA026380
NM_000321.3:c.1573G>A