Canonical Allele Identifier: PA2826017312
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 214
ClinVar RCV Id: RCV000000238 RCV001851506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Glu389del
CA214916
NM_001166057.2:c.1167_1169del