Allele Registry

Canonical Allele Identifier: PA916048652

Gene: BTD HGNC NCBI

ClinVar RCV:

RCV000144059

ClinVar Variation:

156002

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357681.1:p.Asp208Gly	CA278437 NM_001370752.1:c.623A>G