Canonical Allele Identifier: PA2826563079
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg22Cys
CA000257
NM_001276698.3:c.64C>T
CA645588898
NM_001276698.3:c.64_69delinsTGCTGT