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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INO80C, LOC126862726
(P133L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
INO80C, LOC126862726
Single nucleotide variant
(intron variant)
not provided
GBenign