Canonical Allele Identifier: PA107653
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 208
ClinVar RCV Id: RCV000000232 RCV000520088
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Asp276Asn
CA214908
NM_000285.4:c.826G>A