Canonical Allele Identifier: PA658707268
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 489392
ClinVar RCV Id: RCV000579179 RCV001860019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003468.2:p.Arg160His
CA5945875
NM_003477.3:c.479G>A