Canonical Allele Identifier: PA2826197014
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2464471
ClinVar RCV Id: RCV003201947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Pro355Leu
CA2167768
NM_001195129.2:c.1064C>T