Allele Registry

Canonical Allele Identifier: PA916048680

Gene: BTD HGNC NCBI

ClinVar Allele:

36385

ClinVar RCV:

RCV001310478

RCV003323364

RCV003497832

ClinVar Variation:

25048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Val276Gly	CA278272 NM_001370752.1:c.827T>G