Canonical Allele Identifier: PA658800181
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 527902
ClinVar Variation Id: 1718727
ClinVar RCV Id: RCV002301635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Ser37Arg
CA388250346
NM_000321.3:c.109A>C
CA388250351
NM_000321.3:c.111C>G
CA388250352
NM_000321.3:c.111C>A