Allele Registry

Canonical Allele Identifier: PA2826591053

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000819793

ClinVar Variation:

662196

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.His359Arg	CA2277428 NM_001281724.3:c.1076A>G