Allele Registry

Canonical Allele Identifier: PA2826590818

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021962

ClinVar Variation:

25040

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Ile235Thr	CA278258 NM_001281724.3:c.704T>C