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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PCK1
(C192R)
Single nucleotide variant
(missense variant)
Phosphoenolpyruvate carboxykinase deficiency, cytosolic
GPathogenic
PCK1
Single nucleotide variant
(splice donor variant)
Phosphoenolpyruvate carboxykinase deficiency, cytosolic
GLikely pathogenic
PCK1
(P423L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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