Canonical Allele Identifier: PA915959951
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 825440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala17Val
CA388250226
NM_000321.3:c.50C>T