Canonical Allele Identifier: PA175009
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 162380
ClinVar RCV Id: RCV000149774 RCV000149775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Asp368His
CA175008
NM_152778.4:c.1102G>C