Canonical Allele Identifier: PA105514
Gene: MPI HGNC NCBI

Linked Data

ClinVar Variation Id: 2676668
ClinVar RCV Id: RCV003470180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002426.1:p.Tyr255Cys
CA393175958
NM_002435.3:c.764A>G