Canonical Allele Identifier: PA2825607368
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528248
ClinVar Variation Id: 568285

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg158Leu
CA397842028
NM_001126114.3:c.473G>T
CA645589033
NM_001126114.3:c.473_474delinsTT