Canonical Allele Identifier: PA167759
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142206

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Arg110Cys
CA000119
NM_001126113.3:c.328C>T
CA645589283
NM_001126113.3:c.327_328delinsTT