Canonical Allele Identifier: PA2826562031
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 188060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Val38Met
CA000285
NM_001276697.3:c.112G>A