This allele contains a missense mutation resulting from a C to T transition at coding nucleotide 2656 producing an amino acid substitution of arginine with tryptophan at codon 886 (p.R886W). (J:93008)
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This allele contains a missense mutation resulting from a C to T transition at coding nucleotide 2656 producing an amino acid substitution of arginine with tryptophan at codon 886 (p.R886W). (J:93008)