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Links from Gene

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIAO2B, LOC130059167
(P56R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CIAO2B, LOC130059168
(P38L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
CIAO2B, LOC130059168
(E33G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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