Canonical Allele Identifier: PA107672
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 213
ClinVar RCV Id: RCV000000237 RCV002512598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Gly448Arg
CA214915
NM_000285.4:c.1342G>A
CA405220127
NM_000285.4:c.1342G>C