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C98444Level 7

NRAS NM_002524.4:c.183A>T

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A nucleotide substitution at position 183 of the coding sequence of the NRAS gene where adenine has been mutated to thymine.

**Synonyms:** - N-ras c.183A>T - NM_002524.4:c.183A>T - NRAS Q61H (c.183A>T) mutation - NRAS c.183A>T - NRAS1 c.183A>T - Neuroblastoma RAS Viral (v-ras) Oncogene Homolog c.183A>T

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