Canonical Allele Identifier: PA2826762549
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 989848
ClinVar RCV Id: RCV001277749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276084.1:p.Thr261Ala
CA393175994
NM_001289155.2:c.781A>G