Allele Registry

Canonical Allele Identifier: PA2826591851

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000021965

ClinVar Variation:

25043

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Trp252Gly	CA278262 NM_001281725.2:c.754T>G