Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.152865888G>ACA341091NSDHLc.613G>A (p.Gly205Ser)
c.661G>A (p.Gly221Ser)
 ClinVar dbSNP
Xg.152865888G=CA2466153392NSDHLc.613G= (p.Gly205=)
c.661G= (p.Gly221=)
 dbSNP

Number of alleles fetched