Canonical Allele Identifier: PA658668157
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 459182
ClinVar RCV Id: RCV000539474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Ile69Met
CA369608351
NM_002769.5:c.207C>G