Canonical Allele Identifier: PA915989189
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328822
ClinVar RCV Id: RCV000315182 RCV000884956
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Asp87Asn
CA9364428
NM_001166056.2:c.259G>A