Canonical Allele Identifier: PA2830293944
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 943332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689991.1:p.Val347Ala
CA358171944
NM_152778.4:c.1040T>C