Canonical Allele Identifier: PA2826016874
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 328802
ClinVar RCV Id: RCV000300960 RCV001850752 RCV002521206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Gly308Ser
CA9364023
NM_001166056.2:c.922G>A