Canonical Allele Identifier: PA2828443373
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2152899
ClinVar RCV Id: RCV003077335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Ile290Thr
CA3077278
NM_001371595.1:c.869T>C