Canonical Allele Identifier: PA2828492316
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 431131
ClinVar RCV Id: RCV000496155 RCV002222533
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Arg94His
CA3077486
NM_001371590.1:c.281G>A