Canonical Allele Identifier: PA2828444740
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2193941
ClinVar RCV Id: RCV002624151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Met391Val
CA358171340
NM_001371596.2:c.1171A>G