Canonical Allele Identifier: PA2828443302
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 660078
ClinVar RCV Id: RCV000817206 RCV001830792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Val252Ile
CA3077308
NM_001371595.1:c.754G>A