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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRKCG
(G118D)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PRKCG
(R239W)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 14
GUncertain significance