Canonical Allele Identifier: PA645413687
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 428669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Gly449Arg
CA388162556
NM_000321.3:c.1345G>A
CA388162557
NM_000321.3:c.1345G>C