Canonical Allele Identifier: PA2826561487
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769320
ClinVar RCV Id: RCV003510368
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ser221_Ser222delinsCys
CA2697552063
NM_001276696.3:c.662_664del