Canonical Allele Identifier: PA2826762901
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 500792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276086.1:p.Gly189Ser
CA7662536
NM_001289157.2:c.565G>A