Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.112228649A>GCA114321PTSc.139A>G (p.Asn47Asp)
c.-66A>G (n.-66A>G)
n.214A>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.112228649A=CA2000617641PTSc.139A= (p.Asn47=)
c.-66A= (n.-66A=)
n.214A=
 dbSNP

Number of alleles fetched