Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.79599008G>ACA396535004MAFc.895C>T (p.Arg299Cys)
n.2945C>T
ClinVar dbSNP
16g.79599008G>TCA199634MAFc.895C>A (p.Arg299Ser)
n.2945C>A
ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched