Canonical Allele Identifier: PA2829290062
Gene: DBT HGNC NCBI

Linked Data

ClinVar Variation Id: 2918262
ClinVar RCV Id: RCV003637567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001386901.1:p.Leu124Phe
CA341337040
NM_001399972.1:c.370C>T