"Fulgent Genetics, Fulgent Genetics"[submitter] AND "NPR2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 521609	NM_003995.4(NPR2):c.830A>G (p.Asn277Ser)	NPR2 (N277S)	Single nucleotide variant (missense variant)	Acromesomelic dysplasia 1, Maroteaux type +3 more	GUncertain significance
Select item 1440810	NM_003995.4(NPR2):c.1123G>A (p.Gly375Ser)	NPR2 (G375S)	Single nucleotide variant (missense variant)	Acromesomelic dysplasia 1, Maroteaux type +2 more	GUncertain significance