Allele Registry

Canonical Allele Identifier: PA101467

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001057

ClinVar Variation:

1002

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Gly429Asp	CA251660 NM_152778.4:c.1286G>A