Canonical Allele Identifier: PA645415708
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328784
ClinVar RCV Id: RCV000397948 RCV002057492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Ile462Thr
CA9363870
NM_000285.4:c.1385T>C