Canonical Allele Identifier: PA2828443520
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1002
ClinVar RCV Id: RCV000001057
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Gly335Asp
CA251660
NM_001371595.1:c.1004G>A