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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COMP
(N555K)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic
COMP
(D374del)
Microsatellite
(inframe_deletion)
not provided
+1 more
GPathogenic/Likely pathogenic