Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.6110484T>CCA228563VWFc.422A>G (p.Asp141Gly)
c.*481A>G (n.*481A>G)
n.420+31A>G
 ClinVar dbSNP
12g.6110484T=CA2013916464VWFc.422A= (p.Asp141=)
c.*481A= (n.*481A=)
n.420+31A=
 dbSNP

Number of alleles fetched