Canonical Allele Identifier: PA891855343
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 578568
ClinVar RCV Id: RCV000701619
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002426.1:p.Gln15His
CA272821715
NM_002435.3:c.45G>C
CA393169024
NM_002435.3:c.45G>T