Canonical Allele Identifier: PA2573230020
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 1352733
ClinVar RCV Id: RCV002039914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003468.2:p.Trp51Arg
CA380124041
NM_003477.3:c.151T>A
CA380124042
NM_003477.3:c.151T>C