Canonical Allele Identifier: PA154794
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 130047
ClinVar RCV Id: RCV000118074 RCV000313428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003610.2:p.Arg833Gln
CA154793
NM_003619.4:c.2498G>A