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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL41
(R223S)
Single nucleotide variant
(missense variant)
Nemaline myopathy 9
GUncertain significance
KLHL41
(S511P)
Single nucleotide variant
(missense variant)
Nemaline myopathy 9
GUncertain significance