Allele Registry

Canonical Allele Identifier: PA2580102951

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000819793

ClinVar Variation:

662196

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.His379Arg	CA2277428 NM_000060.4:c.1136A>G