Allele Registry

Canonical Allele Identifier: PA2825028203

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV001313934

ClinVar Variation:

1015113

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Arg148Gly	CA351605800 NM_000060.4:c.442C>G