Canonical Allele Identifier: PA916006429
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Leu93Pro
CA000398
NM_001276699.3:c.278T>C