Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.73413587G>CCA99705776ALBc.1011G>C (p.Lys337Asn)
c.666G>C (p.Lys222Asn)
c.435G>C (p.Lys145Asn)
c.*290G>C (p.=)
n.331G>C
c.561G>C (p.Lys187Asn)
n.14G>C
n.697G>C
n.544G>C
c.491-1519G>C (p.=)
c.487-1515G>C (p.=)
dbSNP
4g.73413587G>TCA127892ALBc.1011G>T (p.Lys337Asn)
c.666G>T (p.Lys222Asn)
c.435G>T (p.Lys145Asn)
c.*290G>T (p.=)
n.331G>T
c.561G>T (p.Lys187Asn)
n.14G>T
n.697G>T
n.544G>T
c.491-1519G>T (p.=)
c.487-1515G>T (p.=)
ClinVar dbSNP ExAC gnomAD

Number of alleles fetched