C3714580[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 645005	NM_000069.3(CACNA1S):c.3983T>G (p.Ile1328Ser)	CACNA1S (I1328S)	Single nucleotide variant (missense variant)	Hypokalemic periodic paralysis, type 1 +4 more	GUncertain significance
Select item 1320866	NM_000069.3(CACNA1S):c.550G>A (p.Val184Met)	CACNA1S (V184M)	Single nucleotide variant (missense variant)	Congenital myopathy 18 +4 more	GUncertain significance