Canonical Allele Identifier: PA658663901
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 457149

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Arg168His
CA364657743
NM_183050.3:c.503G>A