Canonical Allele Identifier: PA2826562051
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127818

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg43Cys
CA000288
NM_001276697.3:c.127C>T