Canonical Allele Identifier: PA2828464569
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 214290
ClinVar RCV Id: RCV000199657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358969.1:p.Asn120Ser
CA324201
NM_001372040.1:c.359A>G