Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225646C>G	CA125452	HBB	c.396G>C (p.Gln132His) c.212G>C (n.212G>C)	ClinVar dbSNP
11	g.5225646C=	CA1949564536	HBB	c.396G= (p.Gln132=) c.212G= (n.212G=)	dbSNP

Number of alleles fetched