Canonical Allele Identifier: PA2828444826
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 663594
ClinVar RCV Id: RCV000821501 RCV001272730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Ile426Met
CA3077258
NM_001371596.2:c.1278A>G