Canonical Allele Identifier: PA2826016802
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 3211412
ClinVar RCV Id: RCV004505800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Met236Thr
CA405224778
NM_001166056.2:c.707T>C