ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826197012
Gene: PRSS56
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1368444
ClinVar RCV Id:
RCV001874413
RCV002551028
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001182058.1:p.Pro354Ala
CA2167766
NM_001195129.2:c.1060C>G