MYCN NM_005378.6:c.131C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 131 of the coding sequence of the MYCN gene where cytosine has been mutated to thymine.

**Synonyms:** - MYCN Proto-Oncogene, bHLH Transcription Factor c.131C>T - MYCN c.131C>T - N-myc c.131C>T - NMYC c.131C>T - NM_005378.6:c.131C>T - bHLHe37 c.131C>T - v-Myc Avian Myelocytomatosis Viral Oncogene Neuroblastoma Derived Homolog c.131C>T