Canonical Allele Identifier: PA2826016637
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 1060300
ClinVar RCV Id: RCV001369711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Gly6Arg
CA9364547
NM_001166056.2:c.16G>C
CA9364548
NM_001166056.2:c.16G>A