Allele Registry

Canonical Allele Identifier: PA2826016923

Gene: PEPD HGNC NCBI

ClinVar Allele:

15255

ClinVar RCV:

RCV000000240

ClinVar Variation:

216

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159528.1:p.Glu371Lys	CA214918 NM_001166056.2:c.1111G>A