Allele Registry

Canonical Allele Identifier: PA2828444581

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000640463

RCV001829793

ClinVar Variation:

533369

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358525.1:p.Val321Ile	CA3077331 NM_001371596.2:c.961G>A