Canonical Allele Identifier: PA2826016887
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328801
ClinVar RCV Id: RCV000403163 RCV002521204 RCV002521205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Pro324Leu
CA9364011
NM_001166056.2:c.971C>T