TP53 NM_000546.5:c.396G>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 396 of the coding sequence of the TP53 gene where guanine has been mutated to cytosine.

**Synonyms:** - LFS1 c.396G>C - Li-Fraumeni Syndrome c.396G>C - NM_000546.5:c.396G>C - P53 c.396G>C - TP53 c.396G>C - Tumor Protein p53 c.396G>C