Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
10	g.87714864G>T	CA203030	PAPSS2	c.639+1G>T (n.639+1G>T)	ClinVar dbSNP
10	g.87714864G>A	CA377488029	PAPSS2	c.639+1G>A (n.639+1G>A)	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched