Canonical Allele Identifier: PA2828464269
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 418162
ClinVar RCV Id: RCV000481071
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358968.1:p.Phe137Cys
CA6276663
NM_001372039.1:c.410T>G