Canonical Allele Identifier: PA2826762822
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 1012293
ClinVar RCV Id: RCV001310276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276086.1:p.Gly57Arg
CA393170913
NM_001289157.2:c.169G>C
CA393170917
NM_001289157.2:c.169G>A