ClinVar Miner

List of variants reported as likely pathogenic for Familial hemiplegic migraine

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Total variants: 6
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HGVS dbSNP
NM_000702.3(ATP1A2):c.2143G>A (p.Gly715Arg) rs1553245771
NM_000702.3(ATP1A2):c.2434G>C (p.Asp812His)
NM_000702.3(ATP1A2):c.2564G>A (p.Gly855Glu) rs149144720
NM_000702.3(ATP1A2):c.2810G>A (p.Arg937His) rs1553245943
NM_000702.3(ATP1A2):c.2876C>T (p.Thr959Met) rs1226796744
NM_000702.3(ATP1A2):c.2936C>T (p.Pro979Leu) rs121918615

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