Allele Registry

Canonical Allele Identifier: PA278438

Gene: BTD HGNC NCBI

ClinVar Allele:

165806

ClinVar RCV:

RCV000144059

ClinVar Variation:

156002

HGVS (amino-acid)	Matching Registered Transcripts
NP_000051.1:p.Asp228Gly	CA278437 NM_000060.4:c.683A>G