Canonical Allele Identifier: PA214917
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 214
ClinVar RCV Id: RCV000000238 RCV001851506
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Glu453del
CA214916
NM_000285.4:c.1359_1361del