Canonical Allele Identifier: PA2826026010
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 286347
ClinVar RCV Id: RCV000342110 RCV000406992 RCV000676187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159630.1:p.Arg23Cys
CA5945726
NM_001166158.2:c.67C>T
CA2740130087
NM_001166158.2:c.63_67delinsTGGCT