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Mutations on the Protein: NP_001029031 From Positions: 348 To 380

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0
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OMIM Disease: 609575.0013
p.ALA371THR
N/A
N/A
VLCAD DEFICIENCY


OMIM Disease: 609575.0010
p.ARG365HIS
N/A
N/A
VLCAD DEFICIENCY


OMIM Disease: 609575.0009
p.GLY356ASP
N/A
N/A
VLCAD DEFICIENCY






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