Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154966483A>GCA414916092F8c.1214T>C (p.Ile405Thr)
c.*1090T>C (n.*1090T>C)
n.34T>C
c.1109T>C (p.Ile370Thr)
 ClinVar dbSNP
Xg.154966483A>CCA255098F8c.1214T>G (p.Ile405Ser)
c.*1090T>G (n.*1090T>G)
n.34T>G
c.1109T>G (p.Ile370Ser)
 ClinVar dbSNP

Number of alleles fetched