Canonical Allele Identifier: PA2826197011
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 1556974
ClinVar RCV Id: RCV002188167 RCV003923503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Ser340Phe
CA2167765
NM_001195129.2:c.1019C>T