Canonical Allele Identifier: PA224258
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 96569
ClinVar RCV Id: RCV000082727

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Tyr383Asp
CA224256
NM_183050.3:c.1147T>G