Canonical Allele Identifier: PA2828492852
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_001358520.1:p.Arg139His
CA3077486
NM_001371591.1:c.416G>A