Canonical Allele Identifier: PA2741874174
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2601813
ClinVar RCV Id: RCV003359511
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Pro355Arg
CA66949007
NM_001369848.1:c.1064C>G