Canonical Allele Identifier: PA2826953252
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_001302465.1:p.Pro326Ser
CA122949
NM_001315536.2:c.976C>T