Canonical Allele Identifier: PA2828493052
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995503
ClinVar RCV Id: RCV002819326
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Gly342Arg
CA358172022
NM_001371591.1:c.1024G>C
CA358172024
NM_001371591.1:c.1024G>A