Allele Registry

Chr	Mutation (hg38)	CAid	Gene	Transcript	Linkouts
12	g.80708053G>T	CA123770	MYF6	c.334G>T (p.Ala112Ser)	ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12	g.80708053G=	CA2049373586	MYF6	c.334G= (p.Ala112=)	dbSNP

Number of alleles fetched