Canonical Allele Identifier: PA2825971478
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Arg28His
CA219358
NM_001164278.2:c.83G>A