Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.10793799G>ACA248603DNM2n.1260G>A
c.1072G>A (p.Gly358Arg)
c.328G>A (p.Gly110Arg)
n.432G>A
ClinVar dbSNP
19g.10793799G=CA2322610448DNM2n.1260G=
c.1072G= (p.Gly358=)
c.328G= (p.Gly110=)
n.432G=
dbSNP

Number of alleles fetched