Allele Registry

Canonical Allele Identifier: PA2828448729

Gene: BTD HGNC NCBI

ClinVar Allele:

36339

ClinVar RCV:

RCV000021920

RCV000755882

ClinVar Variation:

25001

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Arg102Gly	CA278195 NM_001370752.1:c.304A>G