Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154987237C>ACA255069F8c.670G>T (p.Gly224Trp)
c.*456G>T (n.*456G>T)
c.565G>T (p.Gly189Trp)
 ClinVar dbSNP
Xg.154987237C=CA2466854875F8c.670G= (p.Gly224=)
c.*456G= (n.*456G=)
c.565G= (p.Gly189=)
 dbSNP

Number of alleles fetched