Canonical Allele Identifier: PA2828443261
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1909906
ClinVar RCV Id: RCV002600537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Ile240Thr
CA358172115
NM_001371595.1:c.719T>C