Canonical Allele Identifier: PA2827026594
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96594

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305904.1:p.Cys107Arg
CA224312
NM_001318975.1:c.319T>C