TP53 NM_000546.5:c.394A>G

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 394 of the coding sequence of the TP53 gene where alanine has been mutated to guanine.

**Synonyms:** - LFS1 c.394A>G - Li-Fraumeni Syndrome c.394A>G - NM_000546.5:c.394A>G - P53 c.394A>G - TP53 c.394A>G - Tumor Protein p53 c.394A>G