Canonical Allele Identifier: PA174727
Gene: PRSS22 HGNC NCBI

Linked Data

ClinVar Variation Id: 161756
ClinVar RCV Id: RCV000149292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071402.1:p.Arg269His
CA023280
NM_022119.4:c.806G>A