Canonical Allele Identifier: PA2826762801
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 1033919
ClinVar RCV Id: RCV001336465
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276086.1:p.Ala32Val
CA393169350
NM_001289157.2:c.95C>T