Canonical Allele Identifier: PA315944
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 206140

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Ile93Val
CA315943
NM_152778.4:c.277A>G