Allele Registry

Canonical Allele Identifier: PA315963

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000188168

ClinVar Variation:

206150

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Asn148Asp	CA315962 NM_152778.4:c.442A>G