Canonical Allele Identifier: PA2826017090
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 209997
ClinVar RCV Id: RCV000195145 RCV002517036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Ala148Pro
CA347445
NM_001166057.2:c.442G>C