Canonical Allele Identifier: PA214919
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 216
ClinVar RCV Id: RCV000000240
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Amino-acid Alleles

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