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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130068838, ARHGAP4
(H4Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ARHGAP4, LOC130068838
Single nucleotide variant
(intron variant)
not provided
GBenign