Canonical Allele Identifier: PA2826565877
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769320
ClinVar RCV Id: RCV003510368

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser221_Ser222delinsCys
CA2697552063
NM_001276760.3:c.662_664del