MSH2 NP_000242.1:p.A636P

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the amino acid residue at position 636 in DNA mismatch repair protein Msh2 where alanine has been replaced by proline.

**Synonyms:** - DNA Mismatch Repair Protein Msh2 A636P - DNA Mismatch Repair Protein Msh2 Ala636Pro - MSH2 A636P - MSH2 Ala636Pro - MSH2 NP_000242.1:p.Ala636Pro - MSH2 p.A636P - MSH2 p.Ala636Pro - MutS Homolog 2 A636P - MutS Homolog 2 Ala636Pro - MutS Protein Homolog 2 A636P - MutS Protein Homolog 2 Ala636Pro - NP_000242.1:p.A636P - NP_000242.1:p.Ala636Pro