Canonical Allele Identifier: PA2827513707
Gene: MFSD2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1716900
ClinVar RCV Id: RCV002296117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336751.1:p.Thr174Ile
CA339834884
NM_001349822.2:c.521C>T