Canonical Allele Identifier: PA2828444821
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421160
ClinVar RCV Id: RCV001916787
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Leu425Val
CA358171124
NM_001371596.2:c.1273C>G