Allele Registry

Canonical Allele Identifier: PA2826591219

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022008

ClinVar Variation:

25083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.His427Tyr	CA278332 NM_001281724.3:c.1279C>T