Canonical Allele Identifier: PA2826562093
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Thr52Ala
CA16615722
NM_001276697.3:c.154A>G