Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
4	g.154586071C>T	CA126479	FGA	c.1358G>A (p.Ser453Asn) c.644-361G>A (n.644-361G>A)	ClinVar dbSNP
4	g.154586071C=	CA1504943322	FGA	c.1358G= (p.Ser453=) c.644-361G= (n.644-361G=)	dbSNP

Number of alleles fetched