Canonical Allele Identifier: PA2826016804
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_001159528.1:p.Gly237Asp
CA214914
NM_001166056.2:c.710G>A