Allele Registry

Canonical Allele Identifier: PA2826591403

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000998007

ClinVar Variation:

809436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Gly14Arg	CA351602804 NM_001281725.2:c.40G>C