Canonical Allele Identifier: PA2830294036
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 853164
ClinVar RCV Id: RCV001057924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile374Val
CA358171457
NM_152778.4:c.1120A>G