Canonical Allele Identifier: PA2828442378
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1995503
ClinVar RCV Id: RCV002819326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Gly293Arg
CA358172022
NM_001371594.1:c.877G>C
CA358172024
NM_001371594.1:c.877G>A