Allele Registry

Canonical Allele Identifier: PA2828440390

Gene: MFSD8 HGNC NCBI

ClinVar Allele:

16043

ClinVar RCV:

RCV000001059

RCV000188166

ClinVar Variation:

1004

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358521.1:p.Tyr121Cys	CA251663 NM_001371592.1:c.362A>G