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Mutations on the Protein: Q8WWZ3 From Positions: 108 To 118

2
1
0
1


Swiss-Prot Disease: VAR_064835
p.ASP114TYR
N/A
N/A
Ectodermal dysplasia 11A, hypohidrotic/hair/nail type, autosomal dominant (ECTD11A)


OMIM Disease: 606603.0002
p.LEU112ARG
N/A
N/A
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL||DOMINANT






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