Canonical Allele Identifier: PA2826016991
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2683487
ClinVar RCV Id: RCV003480307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Cys437Tyr
CA307568372
NM_001166056.2:c.1310G>A