Allele Registry

Canonical Allele Identifier: PA2826017090

Gene: PEPD HGNC NCBI

ClinVar Allele:

206590

ClinVar RCV:

RCV000195145

RCV002517036

ClinVar Variation:

209997

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159529.1:p.Ala148Pro	CA347445 NM_001166057.2:c.442G>C