Canonical Allele Identifier: PA916047991
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 183170
ClinVar RCV Id: RCV000162038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Gly320Arg
CA186005
NM_001369848.1:c.958G>A
CA350991281
NM_001369848.1:c.958G>C