Canonical Allele Identifier: PA2826016725
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_001159528.1:p.Val143Ile
CA9364357
NM_001166056.2:c.427G>A