Canonical Allele Identifier: PA2826017330
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 2683487
ClinVar RCV Id: RCV003480307
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159529.1:p.Cys414Tyr
CA307568372
NM_001166057.2:c.1241G>A