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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACADVL
(T260M +3 more)
Single nucleotide variant
(missense variant)
Very long chain fatty acid accumulation
+2 more
GPathogenic/Likely pathogenic
ACADVL
(V283A +3 more)
Single nucleotide variant
(missense variant)
Very long chain acyl-CoA dehydrogenase deficiency
GPathogenic
ACADVL
(G441D +3 more)
Single nucleotide variant
(missense variant)
Very long chain acyl-CoA dehydrogenase deficiency
GPathogenic
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