Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.763582C>ACA346989SLC52A3c.989G>T (p.Gly330Val)
c.567+1626G>T (n.567+1626G>T)
n.618+1626G>T
 ClinVar dbSNP
20g.763582C=CA2345349291SLC52A3c.989G= (p.Gly330=)
c.567+1626G= (n.567+1626G=)
n.618+1626G=
 dbSNP

Number of alleles fetched