Canonical Allele Identifier: PA101467
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002
ClinVar RCV Id: RCV000001057
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Gly429Asp
CA251660
NM_152778.4:c.1286G>A