Canonical Allele Identifier: PA2828492505
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 284230
ClinVar RCV Id: RCV000334238 RCV001219362 RCV001833332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Glu291Lys
CA10604727
NM_001371590.1:c.871G>A