Canonical Allele Identifier: PA645413598
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 285560

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Pro6Ser
CA10605156
NM_000321.3:c.16C>T