Allele Registry

Canonical Allele Identifier: PA121798

Gene: DBT HGNC NCBI

ClinVar RCV:

RCV000079957

RCV000179835

RCV002251898

RCV003581558

RCV004566722

ClinVar Variation:

11943

HGVS (amino-acid)	Matching Registered Transcripts
NP_001909.3:p.Phe276Cys	CA121797 NM_001918.4:c.827T>G