Canonical Allele Identifier: PA2826762867
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 14347
ClinVar RCV Id: RCV000015421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276086.1:p.Met138Thr
CA257212
NM_001289157.2:c.413T>C