Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.134475197C>G	CA120901	HPRT1	c.151C>G (p.Arg51Gly) n.309C>G n.109C>G c.169C>G (p.Arg57Gly)	ClinVar dbSNP gnomAD v4
X	g.134475197C>T	CA120902	HPRT1	c.151C>T (p.Arg51Ter) n.309C>T n.109C>T c.169C>T (p.Arg57Ter)	ClinVar dbSNP gnomAD v4

Number of alleles fetched