Canonical Allele Identifier: PA2826196953
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2777777
ClinVar RCV Id: RCV003641122
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Val5Met
CA2167665
NM_001195129.2:c.13G>A