Allele Registry

Canonical Allele Identifier: PA2827195791

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021958

ClinVar Variation:

25036

HGVS (amino-acid)	Matching Registered Transcripts
NP_001310511.1:p.Ala217Thr	CA278250 NM_001323582.1:c.649G>A