Canonical Allele Identifier: PA2828443090
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 967674
ClinVar RCV Id: RCV001242649
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Glu140Gln
CA358175984
NM_001371595.1:c.418G>C