Canonical Allele Identifier: PA2828464906
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 214291
ClinVar RCV Id: RCV000196681
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358970.1:p.Ile163Val
CA321102
NM_001372041.1:c.487A>G