Canonical Allele Identifier: PA347446
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 209997
ClinVar RCV Id: RCV000195145 RCV002517036
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Ala212Pro
CA347445
NM_000285.4:c.634G>C