Canonical Allele Identifier: PA2741874161
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_001356777.1:p.Val5Met
CA2167665
NM_001369848.1:c.13G>A