Canonical Allele Identifier: PA2828464190
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 137086
ClinVar RCV Id: RCV000124681 RCV000676202 RCV001001506 RCV003975102
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358968.1:p.Glu19Gln
CA290592
NM_001372039.1:c.55G>C