Allele Registry

Canonical Allele Identifier: PA2499254652

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001361522

ClinVar Variation:

1053206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358521.1:p.Gly312Ala	CA358173779 NM_001371592.1:c.935G>C