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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALPL
(E191K +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+8 more
GPathogenic/Likely pathogenic
ALPL
(D378V +2 more)
Single nucleotide variant
(missense variant)
ALPL-related disorder
+5 more
GPathogenic
ALPL
(R391H +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic
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