Canonical Allele Identifier: PA2828444706
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 347542
ClinVar RCV Id: RCV000412876 RCV000544218 RCV001828342 RCV002487529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Leu369Phe
CA3077283
NM_001371596.2:c.1107G>C
CA358171529
NM_001371596.2:c.1107G>T