Allele Registry

Canonical Allele Identifier: PA658811273

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000640463

RCV001829793

ClinVar Variation:

533369

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Val321Ile	CA3077331 NM_152778.4:c.961G>A