Canonical Allele Identifier: PA2828463206
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 507544
ClinVar RCV Id: RCV000609491 RCV002062962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358965.1:p.Ala67Thr
CA6276559
NM_001372036.1:c.199G>A