Canonical Allele Identifier: PA2826016923
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 216
ClinVar RCV Id: RCV000000240
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Glu371Lys
CA214918
NM_001166056.2:c.1111G>A