Canonical Allele Identifier: PA2828465043
Gene: DLAT HGNC NCBI

Linked Data

ClinVar Variation Id: 208790
ClinVar RCV Id: RCV000190817 RCV000767878 RCV003317143
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358971.1:p.Phe2Val
CA204916
NM_001372042.1:c.4T>G