Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7172381C>TCA124215INSRc.1177G>A (p.Gly393Arg)
n.1152G>A
c.1255G>A (p.Gly419Arg)
 ClinVar dbSNP
19g.7172381C=CA2320790736INSRc.1177G= (p.Gly393=)
n.1152G=
c.1255G= (p.Gly419=)
 dbSNP

Number of alleles fetched