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Mutations on the Protein: NP_001015051 From Positions: 200 To 225

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0
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OMIM Disease: 600211.0010
p.THR200ALA
N/A
N/A
CLEIDOCRANIAL DYSPLASIA||CLEIDOCRANIAL DYSPLASIA, FORME FRUSTE, DENTAL ANOMALIES ONLY, INCLUDED






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