Allele Registry

Canonical Allele Identifier: PA2828492932

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000188172

RCV000765753

RCV000823577

RCV002311276

ClinVar Variation:

206153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358520.1:p.Ile226Thr	CA315969 NM_001371591.1:c.677T>C