Allele Registry

Canonical Allele Identifier: PA2826589467

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021895

ClinVar Variation:

38487

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Val42Met	CA278152 NM_001281723.3:c.124G>A