Canonical Allele Identifier: PA2828493101
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1921825
ClinVar RCV Id: RCV002613323
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Glu392Asp
CA358171327
NM_001371591.1:c.1176A>T
CA358171328
NM_001371591.1:c.1176A>C