Canonical Allele Identifier: PA2573211670
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368444
ClinVar RCV Id: RCV001874413 RCV002551028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Pro355Ala
CA2167766
NM_001369848.1:c.1063C>G