Allele Registry

Canonical Allele Identifier: PA2828441106

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001056

ClinVar Variation:

1001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358522.1:p.Gly272Asp	CA251659 NM_001371593.1:c.815G>A