Canonical Allele Identifier: PA2826016801
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 208
ClinVar RCV Id: RCV000000232 RCV000520088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Asp235Asn
CA214908
NM_001166056.2:c.703G>A