Canonical Allele Identifier: PA2828442567
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2120001
ClinVar RCV Id: RCV003059164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Ala368Thr
CA358171172
NM_001371594.1:c.1102G>A