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NM_000268.4(NF2):c.169C>T (p.Arg57Ter) - NCBI

NM_000268.4(NF2):c.169C>T (p.Arg57Ter). Allele ID: 18324; Variant type: single nucleotide variant; Variant length: 1 bp; Cytogenetic location: 22q12.2 ...

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