Allele Registry

Canonical Allele Identifier: PA915989189

Gene: PEPD HGNC NCBI

ClinVar RCV:

RCV000315182

RCV000884956

ClinVar Variation:

328822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159528.1:p.Asp87Asn	CA9364428 NM_001166056.2:c.259G>A