Allele Registry

Canonical Allele Identifier: PA2826589629

Gene: BTD HGNC NCBI

ClinVar Allele:

36345

ClinVar RCV:

RCV000021926

ClinVar Variation:

25007

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268652.2:p.Phe129Leu	CA278206 NM_001281723.3:c.385T>C CA351605821 NM_001281723.3:c.387C>G CA351605827 NM_001281723.3:c.387C>A