Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
X	g.38367380T>C	CA224487	OTC	c.167T>C (p.Met56Thr) c.172-298741T>C (n.172-298741T>C) n.259T>C	ClinVar dbSNP gnomAD v4
X	g.38367380T=	CA2424870829	OTC	c.167T= (p.Met56=) c.172-298741T= (n.172-298741T=) n.259T=	dbSNP

Number of alleles fetched