Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.18783126C>ACA404875038COMPc.2155G>T (p.Gly719Cys)
c.1996G>T (p.Gly666Cys)
c.2056G>T (p.Gly686Cys)
ClinVar dbSNP
19g.18783126C>TCA343864COMPc.2155G>A (p.Gly719Ser)
c.1996G>A (p.Gly666Ser)
c.2056G>A (p.Gly686Ser)
ClinVar dbSNP

Number of alleles fetched