Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154902120G>ACA255197F8c.6046C>T (p.Arg2016Trp)
c.5941C>T (p.Arg1981Trp)
 ClinVar dbSNP gnomAD v4
Xg.154902120G=CA2466827646F8c.6046C= (p.Arg2016=)
c.5941C= (p.Arg1981=)
 dbSNP

Number of alleles fetched