Canonical Allele Identifier: PA2825786243
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 304472
ClinVar RCV Id: RCV000287345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128496.2:p.Ser221Gly
CA10630807
NM_001135024.2:c.661A>G