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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PTPN23
(Q428fs +1 more)
Deletion
(frameshift variant)
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
GLikely pathogenic
PTPN23
(L434P +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
GUncertain significance