Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47441875G>ACA275256RAPSNc.737C>T (p.Ala246Val)
c.578C>T (p.Ala193Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.47441875G=CA1969387705RAPSNc.737C= (p.Ala246=)
c.578C= (p.Ala193=)
 dbSNP

Number of alleles fetched