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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KRTAP19-6
(C48Y)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KRTAP19-6
(G33V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KRTAP19-6
(G29V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
KRTAP19-6
(G19R)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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