Allele Registry

Canonical Allele Identifier: PA1139743148

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV001202866

ClinVar Variation:

934468

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358524.1:p.Tyr76Ser	CA3077495 NM_001371595.1:c.227A>C