Canonical Allele Identifier: PA2829359705
Gene: DBT HGNC NCBI

Linked Data

ClinVar Variation Id: 2146776
ClinVar RCV Id: RCV003076849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001909.4:p.Met267Leu
CA969653
NM_001918.5:c.799A>T
CA341337928
NM_001918.5:c.799A>C