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Mutations on the Protein: O14802 From Positions: 626 To 695

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Swiss-Prot Disease: VAR_066519
p.GLY672GLU
N/A
N/A
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism (HLD7)


Swiss-Prot Disease: VAR_066518
p.SER636TYR
N/A
N/A
Leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism (HLD7)


OMIM Disease: 614258.0001
p.GLY672GLU
N/A
N/A
LEUKODYSTROPHY, HYPOMYELINATING, 7, WITH OR WITHOUT OLIGODONTIA AND/OR||HYPOGONADOTROPIC HYPOGONADISM






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