Canonical Allele Identifier: PA2828443303
Gene: MFSD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 943332
ClinVar RCV Id: RCV001213504 RCV001833870
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358524.1:p.Val253Ala
CA358171944
NM_001371595.1:c.758T>C