Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.48980693A>G	CA143722	WNT1	c.624+4A>G (n.624+4A>G)	ClinVar dbSNP gnomAD v4
12	g.48980693A=	CA2034925461	WNT1	c.624+4A= (n.624+4A=)	dbSNP

Number of alleles fetched