Canonical Allele Identifier: PA2826561944
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127815

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His20Tyr
CA000256
NM_001276697.3:c.58C>T
CA645588931
NM_001276697.3:c.57_58delinsTT