Canonical Allele Identifier: PA2826561805
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 652718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Thr290Ile
CA287486504
NM_001276696.3:c.869C>T
CA645587346
NM_001276696.3:c.869_870delinsTT