Canonical Allele Identifier: PA107092
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11876
ClinVar RCV Id: RCV000012651 RCV000487005 RCV003944816
ClinVar Variation Id: 11882
ClinVar RCV Id: RCV000012657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Arg122His
CA256109
NM_002769.5:c.365_366delinsAT
CA341151
NM_002769.5:c.365G>A