Canonical Allele Identifier: PA2826197004
Gene: PRSS56 HGNC NCBI
ClinVar RCV:
RCV002594429
ClinVar Variation:
1916237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Cys256Arg
CA350988150
NM_001195129.2:c.766T>C