Allele Registry

Canonical Allele Identifier: PA2828440988

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV003087228

ClinVar Variation:

2172044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358522.1:p.Leu194Arg	CA358175309 NM_001371593.1:c.581T>G