Canonical Allele Identifier: PA2826016992
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1356741
ClinVar RCV Id: RCV001876794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Met438Val
CA9363856
NM_001166056.2:c.1312A>G