Allele Registry

Canonical Allele Identifier: PA2828441358

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001057

ClinVar Variation:

1002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358522.1:p.Gly391Asp	CA251660 NM_001371593.1:c.1172G>A