Allele Registry

Canonical Allele Identifier: PA107643

Gene: PEPD HGNC NCBI

ClinVar RCV:

RCV000000235

RCV003555875

ClinVar Variation:

211

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