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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NAA50
(P157L +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NAA50
(N153I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
NAA50
(I87M +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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