PRKCA NM_002737.3:c.1387G>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 1387 of the coding sequence of the PRKCA gene where guanine has been mutated to cytosine.

**Synonyms:** - NM_002737.3:c.1387G>C - PKC-alpha c.1387G>C - PKCA c.1387G>C - PKCalpha c.1387G>C - PRKACA c.1387G>C - PRKCA c.1387G>C - Protein Kinase C Alpha c.1387G>C