Canonical Allele Identifier: PA2828444299
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 838564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Ile181Val
CA358176034
NM_001371596.2:c.541A>G