Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154904083T>CCA255033F8c.5821A>G (p.Asn1941Asp)
c.5716A>G (p.Asn1906Asp)
 ClinVar dbSNP
Xg.154904083T=CA2466828195F8c.5821A= (p.Asn1941=)
c.5716A= (p.Asn1906=)
 dbSNP

Number of alleles fetched