Canonical Allele Identifier: PA312367
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 203639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Ile341Asn
CA312365
NM_183050.3:c.1022T>A