Canonical Allele Identifier: PA2826017141
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 3211412
ClinVar RCV Id: RCV004505800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Met213Thr
CA405224778
NM_001166057.2:c.638T>C