Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.153725687G>T	CA415098821	ABCD1	c.421G>T (p.Ala141Ser) n.837G>T	dbSNP
X	g.153725687G>A	CA278381	ABCD1	c.421G>A (p.Ala141Thr) n.837G>A	ClinVar dbSNP COSMIC

Number of alleles fetched