Allele Registry

Canonical Allele Identifier: PA2828088358

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001056

ClinVar Variation:

1001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350449.1:p.Gly243Asp	CA251659 NM_001363520.2:c.728G>A