Canonical Allele Identifier: PA110570
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 183171
ClinVar RCV Id: RCV000162039 RCV001723731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Val302Phe
CA186006
NM_001195129.2:c.904G>T