Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154903968C>ACA255189F8c.5936G>T (p.Gly1979Val)
c.5831G>T (p.Gly1944Val)
 ClinVar dbSNP
Xg.154903968C=CA2466828155F8c.5936G= (p.Gly1979=)
c.5831G= (p.Gly1944=)
 dbSNP

Number of alleles fetched