Canonical Allele Identifier: PA915989200
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328820
ClinVar RCV Id: RCV000348554 RCV002521207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Val79Ile
CA9364357
NM_001166057.2:c.235G>A