Canonical Allele Identifier: PA161788
Gene: RB1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135115
ClinVar RCV Id: RCV000121915 RCV000477348 RCV000569325 RCV003945101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000312.2:p.Pro20Leu
CA026462
NM_000321.3:c.59C>T