Canonical Allele Identifier: PA1139743132
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 848575
ClinVar RCV Id: RCV001052356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358521.1:p.Ala254Ser
CA358175161
NM_001371592.1:c.760G>T