Canonical Allele Identifier: PA645413696
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428699

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Cys489Tyr
CA388162860
NM_000321.3:c.1466G>A