Canonical Allele Identifier: PA2826017315
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1391035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Val391Ile
CA9363878
NM_001166057.2:c.1171G>A