Canonical Allele Identifier: PA2826197009
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 2767336
ClinVar RCV Id: RCV003526520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001182058.1:p.Glu301Asp
CA350990920
NM_001195129.2:c.903G>C
CA350990932
NM_001195129.2:c.903G>T