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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
APTX
(A110V +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GLikely pathogenic
APTX
(A110fs +3 more)
Duplication
(frameshift variant +1 more)
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
GPathogenic