ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4534A>G (p.Thr1512Ala)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne RCV003224932 SCV003920954 likely pathogenic Migraine, familial hemiplegic, 1 2022-12-29 criteria provided, single submitter clinical testing

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