Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
20	g.4699732A>G	CA123092	PRNP	c.512A>G (p.Asn171Ser) c.201A>G (n.201A>G)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20	g.4699732A=	CA2347156586	PRNP	c.512A= (p.Asn171=) c.201A= (n.201A=)	dbSNP

Number of alleles fetched