Canonical Allele Identifier: PA2826026015
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 849007
ClinVar RCV Id: RCV001052882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159630.1:p.Leu33Phe
CA5945733
NM_001166158.2:c.97C>T