Canonical Allele Identifier: PA110705
Gene: PPOX HGNC NCBI

Linked Data

ClinVar Variation Id: 8696
ClinVar RCV Id: RCV000009233 RCV001232723 RCV003324489
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000300.1:p.Arg59Trp
CA340813
NM_000309.5:c.175C>T