Allele Registry

Canonical Allele Identifier: PA2826705708

Gene: MFSD2A HGNC NCBI

ClinVar RCV:

RCV000412568

ClinVar Variation:

372260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274738.1:p.Thr122Met	CA16042266 NM_001287809.2:c.365C>T