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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRF1
(W428S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PRF1
(G149S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+5 more
GPathogenic