Canonical Allele Identifier: PA2826016985
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2160305
ClinVar RCV Id: RCV003075881 RCV004071928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Val427Met
CA9363867
NM_001166056.2:c.1279G>A