Canonical Allele Identifier: PA113498
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 13087
ClinVar RCV Id: RCV000013962 RCV000492717 RCV000510137 RCV000763335 RCV000790652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Arg661Trp
CA026417
NM_000321.3:c.1981C>T