Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.97598790G>ACA203970HOGA1c.227G>A (p.Gly76Asp)
c.212-3067G>A (n.212-3067G>A)
n.608G>A
 ClinVar dbSNP
10g.97598790G=CA1930504630HOGA1c.227G= (p.Gly76=)
c.212-3067G= (n.212-3067G=)
n.608G=
 dbSNP

Number of alleles fetched