Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.59153374G>ACA344770FAM111Ac.1706G>A (p.Arg569His)
c.1586G>A (p.Arg529His)
 ClinVar dbSNP
11g.59153374G=CA1976277329FAM111Ac.1706G= (p.Arg569=)
c.1586G= (p.Arg529=)
 dbSNP

Number of alleles fetched