Allele Registry

Canonical Allele Identifier: PA1139701098

Gene: PRSS1 HGNC NCBI

ClinVar RCV:

RCV001237007

ClinVar Variation:

963042

HGVS (amino-acid)	Matching Registered Transcripts
NP_002760.1:p.Arg122Pro	CA369608951 NM_002769.5:c.365G>C