Canonical Allele Identifier: PA2826560851
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro112Thr
CA000198
NM_001276696.3:c.334C>A