Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.79946568A>GCA177970MBL1P,SFTPDc.92T>C (p.Met31Thr)
n.334-3460A>G
c.131T>C (p.Met44Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.79946568A=CA1922423698MBL1P,SFTPDc.92T= (p.Met31=)
n.334-3460A=
c.131T= (p.Met44=)
 dbSNP

Number of alleles fetched