Allele Registry

Canonical Allele Identifier: PA916048672

Gene: BTD HGNC NCBI

ClinVar Allele:

36382

ClinVar RCV:

RCV000021967

RCV001251702

ClinVar Variation:

25045

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Leu258Pro	CA278266 NM_001370752.1:c.773T>C