Canonical Allele Identifier: PA891860198
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 569809
ClinVar RCV Id: RCV000690525 RCV001830503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Arg482Gln
CA3077223
NM_152778.4:c.1445G>A