Canonical Allele Identifier: PA2830293879
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1909906
ClinVar RCV Id: RCV002600537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile334Thr
CA358172115
NM_152778.4:c.1001T>C