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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALPI
(R136C)
Single nucleotide variant
(missense variant)
Inflammatory bowel disease
GUncertain significance
ALPI
(P28L)
Single nucleotide variant
(missense variant)
Inflammatory bowel disease
GUncertain significance