Canonical Allele Identifier: PA338289
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg290Cys
CA001448
NM_001126114.3:c.868C>T