SDHB NM_003000.2:c.487T>C

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 487 of the coding sequence of the SDHB gene where thymine has been mutated to cytosine.

**Synonyms:** - IP c.487T>C - NM_003000.2:c.487T>C - SDH1 c.487T>C - SDH2 c.487T>C - SDHB c.487T>C - SDHIP c.487T>C - Succinate Dehydrogenase Complex Iron Sulfur Subunit B c.487T>C