Canonical Allele Identifier: PA2826017176
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1397018
ClinVar RCV Id: RCV001903293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Arg247Gln
CA9364076
NM_001166057.2:c.740G>A