Canonical Allele Identifier: PA2826016890
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 209998
ClinVar RCV Id: RCV000194259 RCV003556241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159528.1:p.Leu327Arg
CA347422
NM_001166056.2:c.980T>G