Canonical Allele Identifier: PA2825140557
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2844743
ClinVar RCV Id: RCV003719143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Met277Val
CA405224783
NM_000285.4:c.829A>G