Allele Registry

Canonical Allele Identifier: PA2826591239

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV002651650

ClinVar Variation:

2203322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Val437Met	CA278335 NM_001281724.3:c.1309G>A