Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.147831537A>GCA256961SPINK1c.41T>C (p.Leu14Pro)
 ClinVar dbSNP
5g.147831537A>CCA256962SPINK1c.41T>G (p.Leu14Arg)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched