Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.25007418C>T	CA294628	ARX	c.1141G>A (p.Ala381Thr)	ClinVar dbSNP gnomAD v4
X	g.25007418C=	CA2420207115	ARX	c.1141G= (p.Ala381=)	dbSNP

Number of alleles fetched