Canonical Allele Identifier: PA2826559086
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1793227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ala47Pro
CA397845383
NM_001276695.3:c.139G>C