Canonical Allele Identifier: PA645415675
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_000276.2:p.Gly349Ser
CA9364023
NM_000285.4:c.1045G>A