Canonical Allele Identifier: PA224308
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Arg170Pro
CA224306
NM_183050.3:c.509G>C