"Dr. med. U. Finckh, Human Genetics, Eurofins MVZ"[submitter] AND "SCN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2505545	NM_000334.4(SCN4A):c.5215C>T (p.Arg1739Cys)	GH-LCR, SCN4A (R1739C)	Single nucleotide variant (missense variant)	Hypokalemic periodic paralysis, type 2	GUncertain significance
Select item 2580953	NM_000334.4(SCN4A):c.2017C>G (p.Leu673Val)	SCN4A (L673V)	Single nucleotide variant (missense variant)	Hypokalemic periodic paralysis, type 2 +1 more	GUncertain significance