Canonical Allele Identifier: PA2828443491
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1369280
ClinVar RCV Id: RCV001870549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Ser328Leu
CA358171136
NM_001371595.1:c.983C>T