Canonical Allele Identifier: PA2825619062
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Ser275Phe
CA001234
NM_001126118.1:c.824C>T