Canonical Allele Identifier: PA2827026580
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305904.1:p.Arg100Gly
CA224298
NM_001318975.1:c.298C>G