Allele Registry

Canonical Allele Identifier: PA347423

Gene: PEPD HGNC NCBI

ClinVar Allele:

206589

ClinVar RCV:

RCV000194259

RCV003556241

ClinVar Variation:

209998

HGVS (amino-acid)	Matching Registered Transcripts
NP_000276.2:p.Leu368Arg	CA347422 NM_000285.4:c.1103T>G