Allele Registry

Canonical Allele Identifier: PA2828492294

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001059

RCV000188166

ClinVar Variation:

1004

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358519.1:p.Tyr76Cys	CA251663 NM_001371590.1:c.227A>G