Canonical Allele Identifier: PA645419435
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 370949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_898871.1:p.Ala137Val
CA3902601
NM_183050.3:c.410C>T