Allele Registry

Canonical Allele Identifier: PA2826589633

Gene: BTD HGNC NCBI

ClinVar Allele:

165805

ClinVar RCV:

RCV000144057

RCV000985647

ClinVar Variation:

156001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Thr132Arg	CA278435 NM_001281723.3:c.395C>G