Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.52766446C>TCA10635905MBL2c.*1691G>A (n.*1691G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.52766446C=CA1910257069MBL2c.*1691G= (n.*1691G=)
dbSNP

Number of alleles fetched