Canonical Allele Identifier: PA916024166
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305904.1:p.Arg98Cys
CA224289
NM_001318975.1:c.292C>T