Canonical Allele Identifier: PA2826026018
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 2616749
ClinVar RCV Id: RCV003371883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159630.1:p.Arg39Pro
CA5945738
NM_001166158.2:c.116G>C