C169002Level 6
NT5C2 NM_001134373.2:c.1100G>A
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A nucleotide substitution at position 1100 of the coding sequence of the NT5C2 gene where guanine has been mutated to adenine.
**Synonyms:** - 5'-Nucleotidase, Cytosolic II c.1100G>A - NM_001134373.2:c.1100G>A - NT5B c.1100G>A - NT5C2 c.1100G>A - NT5CP c.1100G>A - PNT5 c.1100G>A - cN-II c.1100G>A
GET
/api/v1/systems/nci_thesaurus/nodes/C169002Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.