Canonical Allele Identifier: PA204917
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 208790
ClinVar RCV Id: RCV000190817 RCV000767878 RCV003317143
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001922.2:p.Val157Gly
CA204916
NM_001931.5:c.470T>G