Canonical Allele Identifier: PA119275
Gene: PRSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8070
ClinVar RCV Id: RCV000008536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002761.1:p.Gly191Arg
CA119273
NM_002770.4:c.571G>A
CA458273422
NM_002770.4:c.571G>C