Canonical Allele Identifier: PA2828088234
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350449.1:p.Tyr121Cys
CA251663
NM_001363520.2:c.362A>G