Allele Registry

Canonical Allele Identifier: PA2828443219

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001056

ClinVar Variation:

1001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358524.1:p.Gly216Asp	CA251659 NM_001371595.1:c.647G>A