Canonical Allele Identifier: PA106729
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 43594
ClinVar RCV Id: RCV000131966 RCV000144665 RCV000149051 RCV000205625 RCV000254692 RCV000442470 RCV000421090 RCV000431786 RCV000432002 RCV000785470 RCV003466889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg273Cys
CA000432
NM_000546.6:c.817C>T