Allele Registry

Canonical Allele Identifier: PA2826590221

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000483575

RCV000675116

ClinVar Variation:

418710

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Gly445Cys	CA2277467 NM_001281723.3:c.1333G>T