Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.68839708G>A	CA121634	EFNB1	c.451G>A (p.Gly151Ser)	ClinVar dbSNP gnomAD v4
X	g.68839708G=	CA2435564164	EFNB1	c.451G= (p.Gly151=)	dbSNP

Number of alleles fetched