Canonical Allele Identifier: PA645413697
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala490Thr
CA028873
NM_000321.3:c.1468G>A