Canonical Allele Identifier: PA891845771
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 580275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Thr12Ser
CA388250196
NM_000321.3:c.34A>T
CA388250198
NM_000321.3:c.35C>G