TP53 NM_000546.5:c.815T>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 815 of the coding sequence of the TP53 gene where thymine has been mutated to cytosine.

**Synonyms:** - LFS1 c.815T>C - Li-Fraumeni Syndrome c.815T>C - NM_000546.5:c.815T>C - P53 c.815T>C - TP53 c.815T>C - Tumor Protein p53 c.815T>C