Allele Registry

Canonical Allele Identifier: PA2827195616

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022030

RCV001251701

RCV002513289

ClinVar Variation:

38483

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.His23Arg	CA278364 NM_001323582.1:c.68A>G