Canonical Allele Identifier: PA645454768
Gene: PRSS12 HGNC NCBI

Linked Data

ClinVar Variation Id: 436425
ClinVar RCV Id: RCV000500179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003610.2:p.Arg716Gln
CA104660185
NM_003619.4:c.2147G>A