Canonical Allele Identifier: PA2828444057
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206140
ClinVar RCV Id: RCV000188156 RCV001857624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Ile93Val
CA315943
NM_001371596.2:c.277A>G