Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.3254567C>GCA280099MEFVc.501G>C (p.Glu167Asp)
c.277+1744G>C (n.277+1744G>C)
n.690G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.3254567C=CA2202664878MEFVc.501G= (p.Glu167=)
c.277+1744G= (n.277+1744G=)
n.690G=
 dbSNP

Number of alleles fetched