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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH2
(P256A +4 more)
Single nucleotide variant
(missense variant)
Long QT syndrome 2
GPathogenic
KCNH2
Single nucleotide variant
(splice donor variant)
Long QT syndrome 2
GPathogenic