Canonical Allele Identifier: PA2573213550
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1597118
ClinVar RCV Id: RCV002105713
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Gln453Arg
CA1492817184
NM_001371591.1:c.1358A>G