Canonical Allele Identifier: PA2826705716
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_001274738.1:p.Thr137Ile
CA339834884
NM_001287809.2:c.410C>T