Canonical Allele Identifier: PA2828463681
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 137087
ClinVar RCV Id: RCV000124682 RCV000962443 RCV001530019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358966.1:p.Glu254Lys
CA290594
NM_001372037.1:c.760G>A