Canonical Allele Identifier: PA2580220038
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2188160
ClinVar RCV Id: RCV002616321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Phe381Ile
CA3077280
NM_001371592.1:c.1141T>A