Canonical Allele Identifier: PA2826566145
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Ser275Phe
CA001234
NM_001276760.3:c.824C>T