Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699853G>C	CA266208	PRNP	c.633G>C (p.Glu211Asp) c.322G>C (n.322G>C)	ClinVar dbSNP
20	g.4699853G=	CA2347156642	PRNP	c.633G= (p.Glu211=) c.322G= (n.322G=)	dbSNP

Number of alleles fetched