Canonical Allele Identifier: PA658654255
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 445857
ClinVar RCV Id: RCV000514704 RCV001146301 RCV001821443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003610.2:p.Leu10Val
CA3056037
NM_003619.4:c.28C>G