Canonical Allele Identifier: PA645440793
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 304451
ClinVar RCV Id: RCV000263590 RCV001672447
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001128496.1:p.Gly5Ser
CA5945661
NM_001135024.1:c.13G>A