ClinVar Miner

Submissions for variant NM_001127222.2(CACNA1A):c.4000A>G (p.Lys1334Glu)

dbSNP: rs121908223

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
UniProtKB/Swiss-Prot	RCV000059299	SCV000090851	not provided	Migraine, familial hemiplegic, 1		no assertion provided	not provided

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