Canonical Allele Identifier: PA2826566198
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 652718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr290Ile
CA287486504
NM_001276760.3:c.869C>T
CA645587346
NM_001276760.3:c.869_870delinsTT