Canonical Allele Identifier: PA2580230283
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_001356777.1:p.Pro356Leu
CA2167768
NM_001369848.1:c.1067C>T