Canonical Allele Identifier: PA269691
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 126797
ClinVar RCV Id: RCV000114689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.His733Tyr
CA026427
NM_000321.3:c.2197C>T