Canonical Allele Identifier: PA891845834
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 584872

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Leu676Ser
CA388166793
NM_000321.3:c.2027T>C