Canonical Allele Identifier: PA2828492951
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 975447
ClinVar RCV Id: RCV001252076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Ser246Cys
CA358175207
NM_001371591.1:c.736A>T