Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.10793833G>TCA10584604DNM2n.1294G>T
c.1106G>T (p.Arg369Leu)
c.362G>T (p.Arg121Leu)
n.466G>T
 ClinVar dbSNP
19g.10793833G>ACA118655DNM2n.1294G>A
c.1106G>A (p.Arg369Gln)
c.362G>A (p.Arg121Gln)
n.466G>A
 ClinVar dbSNP

Number of alleles fetched