Canonical Allele Identifier: PA2828444878
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 418295

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358525.1:p.Met454Thr
CA3077232
NM_001371596.2:c.1361T>C