Allele Registry

Canonical Allele Identifier: PA2826592457

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021909

ClinVar Variation:

24991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268655.2:p.Leu63Ser	CA278175 NM_001281726.2:c.188T>C