Canonical Allele Identifier: PA2828463190
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 289331
ClinVar RCV Id: RCV000406039 RCV000726313 RCV003497843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358965.1:p.Pro42Ala
CA6276535
NM_001372036.1:c.124C>G