Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225636C>G	CA124722	HBB	c.406G>C (p.Ala136Pro) c.222G>C (n.222G>C)	ClinVar dbSNP
11	g.5225636C=	CA1949564431	HBB	c.406G= (p.Ala136=) c.222G= (n.222G=)	dbSNP

Number of alleles fetched