Canonical Allele Identifier: PA645415678
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328801
ClinVar RCV Id: RCV000403163 RCV002521204 RCV002521205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Pro365Leu
CA9364011
NM_000285.4:c.1094C>T