Canonical Allele Identifier: PA2579936932
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2701855
ClinVar RCV Id: RCV003510547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Arg110del
CA645589278
NM_000546.6:c.329_331del