ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4363G>T (p.Val1455Leu)

dbSNP: rs121908237
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000009026 SCV000029242 pathogenic Migraine, familial hemiplegic, 1 1999-07-13 no assertion criteria provided literature only
UniProtKB/Swiss-Prot RCV000009026 SCV000090855 not provided Migraine, familial hemiplegic, 1 no assertion provided not provided
GeneReviews RCV001533162 SCV001748981 not provided Familial hemiplegic migraine no assertion provided literature only Hemiplegic attacks

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