Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186271719T>CCA121763F11c.166T>C (p.Cys56Arg)
n.518T>C
n.499T>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.186271719T=CA1519931951F11c.166T= (p.Cys56=)
n.518T=
n.499T=
 dbSNP

Number of alleles fetched