Allele Registry

Canonical Allele Identifier: PA2828088663

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV000725884

RCV001086515

RCV002317122

ClinVar Variation:

206143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350450.1:p.Pro69Leu	CA315948 NM_001363521.2:c.206C>T