PTCH1 NM_000264.4:c.3583A>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 3583 of the coding sequence of the PTCH1 gene where adenine has been mutated to thymine.

**Synonyms:** - NM_000264.4:c.3583A>T - PTC c.3583A>T - PTC1 c.3583A>T - PTCH c.3583A>T - PTCH1 c.3583A>T - Patched 1 c.3583A>T - Patched Homolog 1 c.3583A>T