Canonical Allele Identifier: PA2741828033
Gene: PRSS53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2510683
ClinVar RCV Id: RCV004286267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034592.1:p.Gln217Arg
CA8020882
NM_001039503.3:c.650A>G