Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.4699570C>TCA256776PRNPc.350C>T (p.Ala117Val)
c.*39C>T (n.*39C>T)
 ClinVar dbSNP
20g.4699570C=CA2347156512PRNPc.350C= (p.Ala117=)
c.*39C= (n.*39C=)
 dbSNP

Number of alleles fetched