Allele Registry

Canonical Allele Identifier: PA2826017069

Gene: PEPD HGNC NCBI

ClinVar RCV:

RCV000000235

RCV003555875

ClinVar Variation:

211

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159529.1:p.Arg120Gln	CA214913 NM_001166057.2:c.359G>A