Allele Registry

Canonical Allele Identifier: PA278267

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021967

RCV001251702

ClinVar Variation:

25045

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Leu278Pro	CA278266 NM_000060.4:c.833T>C