Canonical Allele Identifier: PA2828440443
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1715416
ClinVar RCV Id: RCV002301211
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Ser168Phe
CA358176228
NM_001371592.1:c.503C>T