Allele Registry

Chr	Mutation (hg38)	CAid	Linkouts
13	g.48303724G>T	CA026384	ClinVar dbSNP gnomAD v4
13	g.48303724G>A	CA2622977067	ClinVar dbSNP gnomAD v4
13	g.48303724G=	CA2089949479	dbSNP

Number of alleles fetched