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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TIMM9, TOMM20L
(F67C)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
TIMM9, TOMM20L
(P151T)
Single nucleotide variant
(3 prime UTR variant +2 more)
not specified
GUncertain significance