Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.49453751G>ACA364401069MMUTc.917C>T (p.Ser306Phe)
ClinVar dbSNP gnomAD v4
6g.49453751G>TCA364401067MMUTc.917C>A (p.Ser306Tyr)
ClinVar dbSNP

Number of alleles fetched