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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC30A9
(N419S)
Single nucleotide variant
(missense variant)
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
GUncertain significance
SLC30A9
(I406V)
Single nucleotide variant
(missense variant)
Psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome
GUncertain significance