MSH2 NM_000251.2:c.1906G>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1906 of the coding sequence of the MSH2 gene where guanine has been mutated to cytosine.

**Synonyms:** - HNPCC c.1906G>C - HNPCC1 c.1906G>C - MSH2 c.1906G>C - MutS Homolog 2 c.1906G>C - NM_000251.2:c.1906G>C - Postmeiotic Segregation Increased 1 c.1906G>C