Allele Registry

Canonical Allele Identifier: PA2828444127

Gene: MFSD8 HGNC NCBI

ClinVar Allele:

16043

ClinVar RCV:

RCV000001059

RCV000188166

ClinVar Variation:

1004

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358525.1:p.Tyr121Cys	CA251663 NM_001371596.2:c.362A>G