Canonical Allele Identifier: PA916017213
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 14347
ClinVar RCV Id: RCV000015421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276085.1:p.Met88Thr
CA257212
NM_001289156.2:c.263T>C