Non-synonymous FLT3 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A point mutation in the FLT3 gene that encodes an amino acid substitution in the receptor-type tyrosine-protein kinase FLT3 protein.

**Synonyms:** - FLT3 Missense Mutation - Non-synonymous CD135 Gene Mutation - Non-synonymous FLK2 Gene Mutation - Non-synonymous FLT3 Gene Mutant - Non-synonymous FMS-Related Tyrosine Kinase 3 Gene Mutation