Allele Registry

Canonical Allele Identifier: PA2826591629

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021934

ClinVar Variation:

25014

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Ala142Val	CA278217 NM_001281725.2:c.425C>T