Allele Registry

Canonical Allele Identifier: PA2826589832

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000001978

RCV000445043

ClinVar Variation:

1901

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Asp232Gly	CA278012 NM_001281723.3:c.695A>G