Canonical Allele Identifier: PA2828492482
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 211495
ClinVar RCV Id: RCV000194054 RCV000662085 RCV002517099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358519.1:p.Ile267Thr
CA207954
NM_001371590.1:c.800T>C