Allele Registry

Canonical Allele Identifier: PA2828444209

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000188168

ClinVar Variation:

206150

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358525.1:p.Asn148Asp	CA315962 NM_001371596.2:c.442A>G