Allele Registry

Canonical Allele Identifier: PA2826017230

Gene: PEPD HGNC NCBI

ClinVar Allele:

206589

ClinVar RCV:

RCV000194259

RCV003556241

ClinVar Variation:

209998

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159529.1:p.Leu304Arg	CA347422 NM_001166057.2:c.911T>G