Allele Registry

Canonical Allele Identifier: PA2826589792

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000144059

ClinVar Variation:

156002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Asp208Gly	CA278437 NM_001281723.3:c.623A>G