Canonical Allele Identifier: PA107643
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 211
ClinVar RCV Id: RCV000000235 RCV003555875
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Arg184Gln
CA214913
NM_000285.4:c.551G>A