C3887523[trait identifier] AND "Centre for Inherited Metabolic Disease - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 21017	NM_000018.4(ACADVL):c.1405C>T (p.Arg469Trp)	ACADVL, DVL2 (R469W +3 more)	Single nucleotide variant (missense variant)	Very long chain acyl-CoA dehydrogenase deficiency	GLikely pathogenic FDA Recognized database
Select item 474888	NM_000018.4(ACADVL):c.1468G>C (p.Ala490Pro)	ACADVL, DVL2 (A490P +3 more)	Single nucleotide variant (missense variant)	Very long chain acyl-CoA dehydrogenase deficiency	GLikely pathogenic FDA Recognized database