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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLN5, LOC130009913
(W26*)
Single nucleotide variant
(nonsense)
Neuronal ceroid lipofuscinosis
+1 more
GPathogenic
CLN5
Microsatellite
(3 prime UTR variant +1 more)
not provided
+2 more
GPathogenic