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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PDXK
(R130Q +1 more)
Single nucleotide variant
(missense variant)
Neuropathy, hereditary motor and sensory, type VIc, with optic atrophy
GUncertain significance
LOC130066785, PDXK
Single nucleotide variant
(5 prime UTR variant)
not provided
GBenign