Canonical Allele Identifier: PA2828464609
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 302456
ClinVar RCV Id: RCV000609986 RCV003327393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358969.1:p.Pro189Ser
CA6276773
NM_001372040.1:c.565C>T