Canonical Allele Identifier: PA116398
Gene: MPO HGNC NCBI

Linked Data

ClinVar Variation Id: 3635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000241.1:p.Arg499Cys
CA116396
NM_000250.2:c.1495C>T