Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154966664C>ACA255036F8c.1033G>T (p.Val345Leu)
c.*909G>T (n.*909G>T)
c.928G>T (p.Val310Leu)
 ClinVar dbSNP
Xg.154966664C>GCA337336646F8c.1033G>C (p.Val345Leu)
c.*909G>C (n.*909G>C)
c.928G>C (p.Val310Leu)
 dbSNP

Number of alleles fetched