Allele Registry

Canonical Allele Identifier: PA2827195831

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021967

RCV001251702

ClinVar Variation:

25045

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Leu258Pro	CA278266 NM_001323582.1:c.773T>C