Canonical Allele Identifier: PA2826562351
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Leu93Pro
CA000398
NM_001276697.3:c.278T>C