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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HPDL
(A78S)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
GUncertain significance
HPDL
(T263M)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities
GLikely pathogenic