Canonical Allele Identifier: PA2580230282
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2331628
ClinVar RCV Id: RCV002940475
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Pro299Thr
CA350990848
NM_001369848.1:c.895C>A