Canonical Allele Identifier: PA645413801
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 410950
ClinVar RCV Id: RCV000467563 RCV000566527 RCV003942492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Arg798Trp
CA035443
NM_000321.3:c.2392C>T