Canonical Allele Identifier: PA2580282452
Gene: PDHX HGNC NCBI

Linked Data

ClinVar Variation Id: 2079115
ClinVar RCV Id: RCV002995178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003468.2:p.Gly27Glu
CA380123886
NM_003477.3:c.80G>A