HRAS NM_005343.3:c.35_36delinsTA
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A complex substitution where the nucleotide sequence at positions 35 and 36 of the coding sequence of the HRAS gene has changed from guanine-cytosine to thymine-adenine.
**Synonyms:** - C-H-RAS c.35_36delGCinsTA - C-HA-RAS1 c.35_36delGCinsTA - H-ras c.35_36delGCinsTA - HRAS NM_005343.3:c.35_36GC>TA - HRAS NM_005343.3:c.35_36delGCinsTA - HRAS NM_005343.3:c.35_36delGCinsTA - HRAS c.35_36GC>TA - HRAS c.35_36delGCinsTA - HRAS1 c.35_36delGCinsTA - HRas Proto-Oncogene, GTPase c.35_36delGCinsTA - Ha-ras c.35_36delGCinsTA - Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36delGCinsTA - NM_005343.3:c.35_36GC>TA - NM_005343.3:c.35_36delGCinsTA - NM_005343.3:c.35_36delinsTA - RASH1 c.35_36delGCinsTA - v-Ha-ras Harvey Rat Sarcoma Viral Oncogene Homolog c.35_36delGCinsTA
/api/v1/systems/nci_thesaurus/nodes/C140252Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.