Canonical Allele Identifier: PA116389
Gene: MPO HGNC NCBI

Linked Data

ClinVar Variation Id: 3630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000241.1:p.Ala332Val
CA116387
NM_000250.2:c.995C>T