Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699767A>G	CA123090	PRNP	c.547A>G (p.Thr183Ala) c.236A>G (n.236A>G)	ClinVar dbSNP
20	g.4699767A=	CA2347156601	PRNP	c.547A= (p.Thr183=) c.236A= (n.236A=)	dbSNP

Number of alleles fetched