Allele Registry

Canonical Allele Identifier: PA2573072299

Gene: BTD HGNC NCBI

ClinVar Allele:

36331

ClinVar RCV:

RCV000021911

ClinVar Variation:

24993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357682.1:p.Tyr73Cys	CA278179 NM_001370753.1:c.218A>G