Canonical Allele Identifier: PA2826562519
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141193
ClinVar RCV Id: RCV000129588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg121_Arg124delinsHis
CA000443
NM_001276697.3:c.361_371delinsCA