Canonical Allele Identifier: PA347423
Gene: PEPD HGNC NCBI

Linked Data

ClinVar Variation Id: 209998
ClinVar RCV Id: RCV000194259 RCV003556241
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000276.2:p.Leu368Arg
CA347422
NM_000285.4:c.1103T>G