Canonical Allele Identifier: PA2580230280
Gene: PRSS56 HGNC NCBI
ClinVar RCV:
RCV002594429
ClinVar Variation:
1916237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Cys256Arg
CA350988150
NM_001369848.1:c.766T>C