Allele Registry

Canonical Allele Identifier: PA2828445938

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000144060

ClinVar Variation:

156003

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357587.1:p.Thr214Ile	CA278439 NM_001370658.1:c.641C>T