Allele Registry

Canonical Allele Identifier: PA2580102769

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000998007

ClinVar Variation:

809436

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Gly34Arg	CA351602804 NM_000060.4:c.100G>C