Canonical Allele Identifier: PA2828442608
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026836
ClinVar RCV Id: RCV001327341 RCV001830386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358523.1:p.Ser388Tyr
CA358170980
NM_001371594.1:c.1163C>A