Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.31595191T>CCA256835TTRc.272T>C (p.Val91Ala)
c.176T>C (p.Val59Ala)
n.298T>C
 ClinVar dbSNP
18g.31595191T=CA2293887832TTRc.272T= (p.Val91=)
c.176T= (p.Val59=)
n.298T=
 dbSNP

Number of alleles fetched