Canonical Allele Identifier: PA645415360
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328822
ClinVar RCV Id: RCV000315182 RCV000884956
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Asp87Asn
CA9364428
NM_000285.4:c.259G>A