Allele Registry

Canonical Allele Identifier: PA2825786219

Gene: PDHX HGNC NCBI

ClinVar RCV:

RCV001903613

ClinVar Variation:

1405184

HGVS (amino-acid)	Matching Registered Transcripts
NP_001128496.2:p.Gln188Glu	CA220466391 NM_001135024.2:c.562C>G