Canonical Allele Identifier: PA2826559357
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Val104Met
CA000176
NM_001276695.3:c.310G>A