Allele Registry

Canonical Allele Identifier: PA2826591532

Gene: BTD HGNC NCBI

ClinVar Allele:

36337

ClinVar RCV:

RCV000021918

RCV000759007

RCV002513162

ClinVar Variation:

24999

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Gly94Val	CA278191 NM_001281725.2:c.281G>T