• Mutation; HGNC; HGNC:12766; NSD2; Simple; p.Arg776Met (c.2327G>T); Zygosity=Heterozygous (PubMed=35124168).
  
• Mutation; HGNC; HGNC:12766; NSD2; Simple; p.Glu1099Lys (c.3295G>A); ClinVar=VCV000638278; Zygosity=Heterozygous (PubMed=35124168).
  

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