Canonical Allele Identifier: PA2828493083
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045045
ClinVar RCV Id: RCV001349384 RCV001825951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358520.1:p.Asn372Lys
CA3077281
NM_001371591.1:c.1116T>A
CA358171475
NM_001371591.1:c.1116T>G