Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154969444T>ACA255078F8c.896A>T (p.Asn299Ile)
c.*772A>T (n.*772A>T)
c.791A>T (p.Asn264Ile)
 ClinVar dbSNP
Xg.154969444T=CA2466849016F8c.896A= (p.Asn299=)
c.*772A= (n.*772A=)
c.791A= (p.Asn264=)
 dbSNP

Number of alleles fetched