Allele Registry

Canonical Allele Identifier: PA2827513589

Gene: MFSD2A HGNC NCBI

ClinVar RCV:

RCV000412568

ClinVar Variation:

372260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336750.1:p.Thr157Met	CA16042266 NM_001349821.2:c.470C>T