Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904082T>CCA255184F8c.5822A>G (p.Asn1941Ser)
c.5717A>G (p.Asn1906Ser)
 ClinVar dbSNP
Xg.154904082T=CA2466828194F8c.5822A= (p.Asn1941=)
c.5717A= (p.Asn1906=)
 dbSNP

Number of alleles fetched