Allele Registry

Canonical Allele Identifier: PA2826589785

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000420327

RCV000675128

RCV001251699

RCV001731677

RCV004022351

ClinVar Variation:

381650

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Asp202Asn	CA2277359 NM_001281723.3:c.604G>A