Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.139541099C>G	CA255326	F9	c.301C>G (p.Pro101Ala) c.277+3713C>G (n.277+3713C>G) n.254C>G	ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
X	g.139541099C=	CA2461405472	F9	c.301C= (p.Pro101=) c.277+3713C= (n.277+3713C=) n.254C=	dbSNP

Number of alleles fetched