Allele Registry

Canonical Allele Identifier: PA214919

Gene: PEPD HGNC NCBI

ClinVar Allele:

15255

ClinVar RCV:

RCV000000240

ClinVar Variation:

216

HGVS (amino-acid)	Matching Registered Transcripts
NP_000276.2:p.Glu412Lys	CA214918 NM_000285.4:c.1234G>A