Canonical Allele Identifier: PA107112
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 38366
ClinVar RCV Id: RCV000031923
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Asn29Thr
CA343001
NM_002769.5:c.86A>C