Canonical Allele Identifier: PA2828444802
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1432417
ClinVar RCV Id: RCV001941251
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Leu420Phe
CA358171150
NM_001371596.2:c.1258C>T