Allele Registry

Canonical Allele Identifier: PA2827513701

Gene: MFSD2A HGNC NCBI

ClinVar RCV:

RCV000412568

ClinVar Variation:

372260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336751.1:p.Thr159Met	CA16042266 NM_001349822.2:c.476C>T