Allele Registry

Canonical Allele Identifier: PA2741810601

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV003499571

ClinVar Variation:

2723714

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Arg15Gly	CA2277186 NM_000060.4:c.43A>G