Canonical Allele Identifier: PA2826091110
Gene: PDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 13189
ClinVar RCV Id: RCV000014077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166939.1:p.Pro326Ser
CA122949
NM_001173468.2:c.976C>T