Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.6195859C>TCA362738908F13A1c.1243G>A (p.Val415Ile)
c.1405G>A (p.Val469Ile)
 dbSNP gnomAD v4
6g.6195859C>ACA126630F13A1c.1243G>T (p.Val415Phe)
c.1405G>T (p.Val469Phe)
 ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched