Canonical Allele Identifier: PA1139758014
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 992182

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Ala40Val
CA3902502
NM_183050.3:c.119C>T