Allele Registry

Canonical Allele Identifier: PA2828443218

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001361522

ClinVar Variation:

1053206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358524.1:p.Gly216Ala	CA358173779 NM_001371595.1:c.647G>C