Canonical Allele Identifier: PA2828444298
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014741
ClinVar RCV Id: RCV001313513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Ile181Leu
CA358176036
NM_001371596.2:c.541A>C