"PreventionGenetics, part of Exact Sciences"[submitter] AND "NAPB"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045570	NM_022080.3(NAPB):c.69C>T (p.Ala23=)	NAPB	Single nucleotide variant (synonymous variant +2 more)	NAPB-related disorder	GLikely benign
Select item 709378	NM_022080.3(NAPB):c.65A>G (p.Lys22Arg)	LOC130065540, NAPB (K22R)	Single nucleotide variant (missense variant +2 more)	NAPB-related disorder +1 more	GBenign