Canonical Allele Identifier: PA645436339
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Cys97Arg
CA16620623
NM_001126117.1:c.289T>C