C137952Level 6
Non-synonymous ALK Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in the ALK gene that encodes an amino acid substitution in the ALK tyrosine kinase receptor protein.
**Synonyms:** - ALK Missense Mutation - Non-synonymous ALK Receptor Tyrosine Kinase Gene Mutation - Non-synonymous Anaplastic Lymphoma Kinase Receptor Gene Mutation - Non-synonymous Anaplastic Lymphoma Receptor Tyrosine Kinase Gene Mutation - Non-synonymous CD246 Gene Mutation
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