Canonical Allele Identifier: PA2573072417
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 431131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Arg94His
CA3077486
NM_001371595.1:c.281G>A