Allele Registry

Canonical Allele Identifier: PA2826589533

Gene: BTD HGNC NCBI

ClinVar Allele:

36331

ClinVar RCV:

RCV000021911

ClinVar Variation:

24993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Tyr73Cys	CA278179 NM_001281723.3:c.218A>G