Allele Registry

Canonical Allele Identifier: PA2573072411

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001059

RCV000188166

ClinVar Variation:

1004

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358524.1:p.Tyr76Cys	CA251663 NM_001371595.1:c.227A>G