Canonical Allele Identifier: PA224294
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96587

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Tyr169Cys
CA224292
NM_183050.3:c.506A>G