Canonical Allele Identifier: PA2827026719
Gene: BCKDHB HGNC NCBI

Linked Data

ClinVar Variation Id: 224061
ClinVar RCV Id: RCV000209523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305904.1:p.Thr252Ala
CA354915
NM_001318975.1:c.754A>G