Canonical Allele Identifier: PA645415683
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328797
ClinVar RCV Id: RCV000339838 RCV001859937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Val386Met
CA10651745
NM_000285.4:c.1156G>A