Allele Registry

Canonical Allele Identifier: PA2828088359

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001361522

ClinVar Variation:

1053206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350449.1:p.Gly243Ala	CA358173779 NM_001363520.2:c.728G>C