Allele Registry

Canonical Allele Identifier: PA2826590774

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021958

ClinVar Variation:

25036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268653.2:p.Ala217Thr	CA278250 NM_001281724.3:c.649G>A