Allele Registry

Canonical Allele Identifier: PA2826591862

Gene: BTD HGNC NCBI

ClinVar Allele:

36382

ClinVar RCV:

RCV000021967

RCV001251702

ClinVar Variation:

25045

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Leu258Pro	CA278266 NM_001281725.2:c.773T>C