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Mutations on the Protein: NP_001244303 From Positions: 488 To 517

3
0
0
3


OMIM Disease: 150330.0022
p.GLY496GLY
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME||RESTRICTIVE DERMOPATHY, LETHAL, INCLUDED


OMIM Disease: 150330.0023
p.GLY496SER
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME


OMIM Disease: 150330.0040
p.VAL495VAL
N/A
N/A
HUTCHINSON-GILFORD PROGERIA SYNDROME






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