ClinVar Miner

List of variants in gene KCNH2 studied for Inborn genetic diseases

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Total variants: 3
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HGVS dbSNP
NM_000238.3(KCNH2):c.1681G>A (p.Ala561Thr) rs199472921
NM_000238.3(KCNH2):c.2078T>C (p.Leu693Pro) rs199472983
NM_000238.3(KCNH2):c.2587C>T (p.Arg863Ter) rs773724817

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