Canonical Allele Identifier: PA2826016977
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1391035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Val414Ile
CA9363878
NM_001166056.2:c.1240G>A