Allele Registry

Canonical Allele Identifier: PA2829744329

Gene: BBS9 HGNC NCBI

ClinVar Variation Id: 242248

HGVS (amino-acid)	Matching Registered Transcripts
NP_055266.2:p.Leu739Gln	CA4214668 NM_014451.4:c.2216T>A