Canonical Allele Identifier: PA2826561568
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys236Trp
CA397836936
NM_001276696.3:c.708T>G