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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLPP, LOC130063288
Single nucleotide variant
(intron variant)
Perrault syndrome 3
+1 more
GPathogenic
CLPP
(T145P)
Single nucleotide variant
(missense variant)
Perrault syndrome 3
GPathogenic
CLPP
(C147S)
Single nucleotide variant
(missense variant)
Perrault syndrome 3
GPathogenic
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