Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.38369806T>C	CA224505	OTC	c.227T>C (p.Leu76Ser) c.172-296315T>C (n.172-296315T>C) n.319T>C	ClinVar dbSNP gnomAD v4
X	g.38369806T=	CA2424871657	OTC	c.227T= (p.Leu76=) c.172-296315T= (n.172-296315T=) n.319T=	dbSNP

Number of alleles fetched