Canonical Allele Identifier: PA2828440414
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 431131
ClinVar RCV Id: RCV000496155 RCV002222533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Arg139His
CA3077486
NM_001371592.1:c.416G>A