Canonical Allele Identifier: PA107643
Gene: PEPD HGNC NCBI
ClinVar Allele:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Arg184Gln
CA214913
NM_000285.4:c.551G>A