Canonical Allele Identifier: PA2828461311
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 534585
ClinVar RCV Id: RCV000642190
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358960.1:p.Ile119Val
CA382598011
NM_001372031.1:c.355A>G