Allele Registry

Canonical Allele Identifier: PA645408417

Gene: MFSD2A HGNC NCBI

ClinVar RCV:

RCV000412568

ClinVar Variation:

372260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129965.1:p.Thr172Met	CA16042266 NM_001136493.3:c.515C>T