Allele Registry

Canonical Allele Identifier: PA2826017081

Gene: PEPD HGNC NCBI

ClinVar Allele:

15257

ClinVar RCV:

RCV000000242

ClinVar Variation:

218

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159529.1:p.Ser138Phe	CA339805 NM_001166057.2:c.413C>T