KIT NM_000222.2:c.1727T>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1727 of the coding sequence of the KIT gene where thymine has been mutated to cytosine.

**Synonyms:** - CD117 c.1727T>C - KIT L576P (c.1727T>C) mutation - KIT Proto-Oncogene Tyrosine Protein Kinase c.1727T>C - KIT c.1727T>C - NM_000222.2:c.1727T>C - c-KIT c.1727T>C - v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog c.1727T>C