Canonical Allele Identifier: PA2828464871
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 452714
ClinVar RCV Id: RCV000518970 RCV003333076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358970.1:p.Asp123Tyr
CA382598087
NM_001372041.1:c.367G>T