Allele Registry

Canonical Allele Identifier: PA2827195659

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021911

ClinVar Variation:

24993

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Tyr73Cys	CA278179 NM_001323582.1:c.218A>G