Canonical Allele Identifier: PA2741874161
Gene: PRSS56 HGNC NCBI
ClinVar RCV:
RCV003641122
ClinVar Variation:
2777777
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Val5Met
CA2167665
NM_001369848.1:c.13G>A