Allele Registry

Canonical Allele Identifier: PA645415675

Gene: PEPD HGNC NCBI

ClinVar Allele:

343225

ClinVar RCV:

RCV000300960

RCV001850752

RCV002521206

ClinVar Variation:

328802

HGVS (amino-acid)	Matching Registered Transcripts
NP_000276.2:p.Gly349Ser	CA9364023 NM_000285.4:c.1045G>A