Canonical Allele Identifier: PA2828462840
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1977862
ClinVar RCV Id: RCV002736836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358964.1:p.Tyr85Asp
CA382596528
NM_001372035.1:c.253T>G