Canonical Allele Identifier: PA2826762848
Gene: MPI HGNC NCBI
ClinVar Allele:
29385
ClinVar RCV:
RCV000015420
ClinVar Variation:
14346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276086.1:p.Ser102Leu
CA257211
NM_001289157.2:c.305C>T