Allele Registry

Canonical Allele Identifier: PA278180

Gene: BTD HGNC NCBI

ClinVar Allele:

36331

ClinVar RCV:

RCV000021911

ClinVar Variation:

24993

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Tyr93Cys	CA278179 NM_000060.4:c.278A>G