Canonical Allele Identifier: PA2826562576
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg131Cys
CA001448
NM_001276697.3:c.391C>T