F2 NM_000506.4:c.*97G>A

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position *97 in the 3' untranslated region of the F2 gene where guanine has been mutated to adenine.

**Synonyms:** - Coagulation Factor II (Thrombin) 20210G>A - Coagulation Factor II, Thrombin 20210G>A - F2 20210G-A - F2 20210G>A - F2 G20210A - F2 c.*97G>A - F2 c.20210G>A - F2 g.25313G>A - F2, 20210G-A - Factor II 20210G-A Mutation - NG_008953.1:g.25313G>A - NM_000506.4:c.*97G>A - Prothrombin 20210G>A - Prothrombin G20210A