Canonical Allele Identifier: PA2828462199
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 137087

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358962.1:p.Glu310Lys
CA290594
NM_001372033.1:c.928G>A