Canonical Allele Identifier: PA2828492356
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014741
ClinVar RCV Id: RCV001313513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Ile136Leu
CA358176036
NM_001371590.1:c.406A>C