Canonical Allele Identifier: PA2828461616
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 2289838
ClinVar RCV Id: RCV002837054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358961.1:p.Arg44Leu
CA6276527
NM_001372032.1:c.131G>T