Canonical Allele Identifier: PA645415363
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328820
ClinVar RCV Id: RCV000348554 RCV002521207
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Val143Ile
CA9364357
NM_000285.4:c.427G>A