Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904871C>TCA255169F8c.5526G>A (p.Met1842Ile)
c.5421G>A (p.Met1807Ile)
 ClinVar dbSNP
Xg.154904871C=CA2466828435F8c.5526G= (p.Met1842=)
c.5421G= (p.Met1807=)
 dbSNP

Number of alleles fetched