Allele Registry

Canonical Allele Identifier: PA101556

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000001059

RCV000188166

ClinVar Variation:

1004

HGVS (amino-acid)	Matching Registered Transcripts
NP_689991.1:p.Tyr121Cys	CA251663 NM_152778.4:c.362A>G