Canonical Allele Identifier: PA2826566813
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528248
ClinVar Variation Id: 568285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg119Leu
CA397842028
NM_001276761.3:c.356G>T
CA645589033
NM_001276761.3:c.356_357delinsTT