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Mutations on the Protein: P50148 From Positions: 180 To 197

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0
0
1






OMIM Disease: 600998.0001
p.ARG183GLN
N/A
N/A
STURGE-WEBER SYNDROME, SOMATIC, MOSAIC||CAPILLARY MALFORMATIONS, CONGENITAL, 1, SOMATIC, MOSAIC, INCLUDED






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