Allele Registry

Canonical Allele Identifier: PA2826590199

Gene: BTD HGNC NCBI

ClinVar Variation Id: 458806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Tyr434Cys	CA2277463 NM_001281723.3:c.1301A>G