Canonical Allele Identifier: PA2828443376
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2077803
ClinVar RCV Id: RCV002985707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Trp293Cys
CA358171360
NM_001371595.1:c.879G>T
CA358171362
NM_001371595.1:c.879G>C