Canonical Allele Identifier: PA338288
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Arg290Cys
CA001448
NM_001126113.3:c.868C>T