Canonical Allele Identifier: PA2828088404
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 943332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350449.1:p.Val280Ala
CA358171944
NM_001363520.2:c.839T>C