Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.94381078A>GCA127617SERPINA1c.710T>C (p.Val237Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.94381078A>CCA390848914SERPINA1c.710T>G (p.Val237Gly)
 dbSNP gnomAD v4
14g.94381078A=CA127619SERPINA1c.710T= (p.Val237=)
 ClinVar dbSNP

Number of alleles fetched