Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
11	g.5225608T>A	CA125476	HBB	c.434A>T (p.Lys145Met) c.250A>T (n.250A>T)	ClinVar dbSNP
11	g.5225608T=	CA1949564150	HBB	c.434A= (p.Lys145=) c.250A= (n.250A=)	dbSNP

Number of alleles fetched