NTRK1 NM_001012331.1:c.1792C>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1792 of the coding sequence of the NTRK1 gene where cytosine has been mutated to thymine.

**Synonyms:** - MTC c.1792C>T - NM_001012331.1:c.1792C>T - NTRK1 c.1792C>T - Neurotrophic Receptor Tyrosine Kinase 1 c.1792C>T - TRK c.1792C>T - TRK1 c.1792C>T - Trk-A c.1792C>T - TrkA c.1792C>T - p140-TrkA c.1792C>T