Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225641A>G	CA125492	HBB	c.401T>C (p.Val134Ala) c.217T>C (n.217T>C)	ClinVar dbSNP
11	g.5225641A=	CA1949564472	HBB	c.401T= (p.Val134=) c.217T= (n.217T=)	dbSNP

Number of alleles fetched