Allele Registry

Canonical Allele Identifier: PA916030233

Gene: MFSD2A HGNC NCBI

ClinVar RCV:

RCV000412568

ClinVar Variation:

372260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336752.1:p.Thr44Met	CA16042266 NM_001349823.2:c.131C>T