List of variants in gene ATP1A2 reported as likely pathogenic for Alternating hemiplegia of childhood 1

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr)	rs181618883	0.00001
NM_000702.4(ATP1A2):c.1133C>A (p.Thr378Asn)	rs28934002
NM_000702.4(ATP1A2):c.1843G>A (p.Gly615Arg)	rs770053423
NM_000702.4(ATP1A2):c.2336G>A (p.Ser779Asn)	rs2101995480

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