Allele Registry

Canonical Allele Identifier: PA2826592518

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021920

RCV000755882

ClinVar Variation:

25001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268655.2:p.Arg102Gly	CA278195 NM_001281726.2:c.304A>G