Allele Registry

Canonical Allele Identifier: PA2580102967

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV003029786

ClinVar Variation:

2113926

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Gly413Arg	CA351608374 NM_000060.4:c.1237G>C