Allele Registry

Canonical Allele Identifier: PA2826589622

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021924

RCV000490188

RCV002513163

RCV003226165

ClinVar Variation:

25005

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Arg128His	CA278201 NM_001281723.3:c.383G>A