Allele Registry

Canonical Allele Identifier: PA2828088488

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001057

ClinVar Variation:

1002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350449.1:p.Gly362Asp	CA251660 NM_001363520.2:c.1085G>A