Canonical Allele Identifier: PA916006449
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Leu98Gln
CA000402
NM_001276699.3:c.293T>A