Allele Registry

Canonical Allele Identifier: PA2826592065

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV001959733

ClinVar Variation:

1431894

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Asn382Asp	CA2277435 NM_001281725.2:c.1144A>G