Canonical Allele Identifier: PA2580220033
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2415035
ClinVar RCV Id: RCV003110454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Gln367Arg
CA358171653
NM_001371592.1:c.1100A>G