Allele Registry

Canonical Allele Identifier: PA2826592305

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000022022

ClinVar Variation:

25097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268654.1:p.Gln491Glu	CA278352 NM_001281725.2:c.1471C>G