Canonical Allele Identifier: PA220668
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 92842
ClinVar RCV Id: RCV000078638 RCV000573514 RCV000810054 RCV003493436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Arg876Cys
CA026444
NM_000321.3:c.2626C>T