Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49453692T>CCA364400752MMUTc.976A>G (p.Arg326Gly)
ClinVar dbSNP gnomAD v4
6g.49453692T>ACA364400750MMUTc.976A>T (p.Arg326Ter)
ClinVar dbSNP

Number of alleles fetched