Canonical Allele Identifier: PA2573167383
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1391035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Val455Ile
CA9363878
NM_000285.4:c.1363G>A