Canonical Allele Identifier: PA2826017081
Gene: PEPD HGNC NCBI
ClinVar RCV:
RCV000000242
ClinVar Variation:
218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Ser138Phe
CA339805
NM_001166057.2:c.413C>T