Canonical Allele Identifier: PA107662
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 212
ClinVar RCV Id: RCV000000236 RCV002512597
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Gly278Asp
CA214914
NM_000285.4:c.833G>A