Canonical Allele Identifier: PA2827026726
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305904.1:p.Leu255Arg
CA224365
NM_001318975.1:c.764T>G