Canonical Allele Identifier: PA107166
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 11878
ClinVar RCV Id: RCV000012653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Lys23Arg
CA341153
NM_002769.5:c.68A>G