Canonical Allele Identifier: PA2826762683
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 989848
ClinVar RCV Id: RCV001277749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276085.1:p.Thr211Ala
CA393175994
NM_001289156.2:c.631A>G