Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47447927A>GCA119259RAPSNc.416T>C (p.Phe139Ser)
 ClinVar dbSNP
11g.47447927A=CA1969378363RAPSNc.416T= (p.Phe139=)
 dbSNP

Number of alleles fetched