Canonical Allele Identifier: PA111844
Gene: PDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 13188
ClinVar RCV Id: RCV000014076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000916.2:p.Tyr132Cys
CA122948
NM_000925.4:c.395A>G