Allele Registry

Canonical Allele Identifier: PA2826590360

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022026

ClinVar Variation:

25101

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Tyr520Cys	CA278359 NM_001281723.3:c.1559A>G