Canonical Allele Identifier: PA101414
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_689991.1:p.Arg139His
CA3077486
NM_152778.4:c.416G>A