Allele Registry

Canonical Allele Identifier: PA2826590905

Gene: BTD HGNC NCBI

ClinVar Allele:

36385

ClinVar RCV:

RCV001310478

RCV003323364

RCV003497832

ClinVar Variation:

25048

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Val276Gly	CA278272 NM_001281724.3:c.827T>G