TP53 NM_000546.5:c.817C>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 817 of the coding sequence of the TP53 gene where cytosine has been mutated to adenine.

**Synonyms:** - LFS1 c.817C>A - Li-Fraumeni Syndrome c.817C>A - NM_000546.5:c.817C>A - P53 c.817C>A - TP53 c.817C>A - Tumor Protein p53 c.817C>A