Canonical Allele Identifier: PA2826197018
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2349842
ClinVar RCV Id: RCV002977301
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Arg364Gly
CA66949043
NM_001195129.2:c.1090C>G