Allele Registry

Canonical Allele Identifier: PA916048663

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021962

ClinVar Variation:

25040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Ile235Thr	CA278258 NM_001370752.1:c.704T>C