Allele Registry

Canonical Allele Identifier: PA2828444420

Gene: MFSD8 HGNC NCBI

ClinVar RCV:

RCV003087228

ClinVar Variation:

2172044

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358525.1:p.Leu232Arg	CA358175309 NM_001371596.2:c.695T>G