TP53 NM_000546.5:c.797G>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 797 of the coding sequence of the TP53 gene where guanine has been mutated to adenine.

**Synonyms:** - LFS1 c.797G>A - Li-Fraumeni Syndrome c.797G>A - NM_000546.5:c.797G>A - P53 c.797G>A - TP53 c.797G>A - Tumor Protein p53 c.797G>A