Canonical Allele Identifier: PA645415686
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328796
ClinVar RCV Id: RCV000284801 RCV000514422
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Arg388His
CA9363969
NM_000285.4:c.1163G>A