Canonical Allele Identifier: PA2826559140
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 186132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Thr63Ile
CA000098
NM_001276695.3:c.188C>T