Canonical Allele Identifier: PA2828463212
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 1977862
ClinVar RCV Id: RCV002736836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358965.1:p.Leu71Arg
CA382596528
NM_001372036.1:c.212T>G