Allele Registry

Canonical Allele Identifier: PA2828088803

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001361522

ClinVar Variation:

1053206

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350450.1:p.Gly205Ala	CA358173779 NM_001363521.2:c.614G>C