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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC4
(T725M +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
GUncertain significance
HDAC4
(K174fs)
Deletion
(frameshift variant)
Neurodevelopmental disorder with central hypotonia and dysmorphic facies
GUncertain significance