Allele Registry

Canonical Allele Identifier: PA2828448562

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000998007

ClinVar Variation:

809436

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Gly14Arg	CA351602804 NM_001370752.1:c.40G>C