Allele Registry

Canonical Allele Identifier: PA2826016874

Gene: PEPD HGNC NCBI

ClinVar RCV:

RCV000300960

RCV001850752

RCV002521206

ClinVar Variation:

328802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159528.1:p.Gly308Ser	CA9364023 NM_001166056.2:c.922G>A