Allele Registry

Canonical Allele Identifier: PA2826589623

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV001313934

ClinVar Variation:

1015113

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Arg128Gly	CA351605800 NM_001281723.3:c.382C>G