The GenomeBrowse view in VarSeq shows a seemingly high-quality alignment evidence for the NM_002769.4(PRSS1):c.86A>T variant in PRSS1 in my exome
The GenomeBrowse view in VarSeq shows a seemingly high-quality alignment evidence for the NM_002769.4(PRSS1):c.86A>T variant in PRSS1 in my exome