Canonical Allele Identifier: PA2826562130
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Val58Leu
CA397839964
NM_001276697.3:c.172G>C
CA397839966
NM_001276697.3:c.172G>T