Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.129963462T>CCA16044297EBF3n.146A>G
c.196A>G (p.Asn66Asp)
n.702A>G
ClinVar dbSNP gnomAD v4
10g.129963462T=CA1945005535EBF3n.146A=
c.196A= (p.Asn66=)
n.702A=
dbSNP

Number of alleles fetched