Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154899946A>GCA255199F8c.6193T>C (p.Trp2065Arg)
c.6088T>C (p.Trp2030Arg)
 ClinVar dbSNP
Xg.154899946A=CA2466827072F8c.6193T= (p.Trp2065=)
c.6088T= (p.Trp2030=)
 dbSNP

Number of alleles fetched