Canonical Allele Identifier: PA2826016905
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328796
ClinVar RCV Id: RCV000284801 RCV000514422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Arg347His
CA9363969
NM_001166056.2:c.1040G>A