Allele Registry

Canonical Allele Identifier: PA2826016801

Gene: PEPD HGNC NCBI

ClinVar Allele:

15247

ClinVar RCV:

RCV000000232

RCV000520088

ClinVar Variation:

208

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159528.1:p.Asp235Asn	CA214908 NM_001166056.2:c.703G>A