Canonical Allele Identifier: PA2828462461
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 534585
ClinVar RCV Id: RCV000642190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358963.1:p.Ile108Val
CA382598011
NM_001372034.1:c.322A>G