Allele Registry

Canonical Allele Identifier: PA2580102964

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV001959733

ClinVar Variation:

1431894

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Asn402Asp	CA2277435 NM_000060.4:c.1204A>G