Canonical Allele Identifier: PA2825121136
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729952

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ala11Val
CA388250193
NM_000321.3:c.32C>T