Canonical Allele Identifier: PA2826090973
Gene: PDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 978592
ClinVar RCV Id: RCV001257311

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166939.1:p.Trp147Ser
CA353361337
NM_001173468.2:c.440G>C