Allele Registry

Canonical Allele Identifier: PA2829744218

Gene: BBS9 HGNC NCBI

ClinVar Variation Id: 166740

HGVS (amino-acid)	Matching Registered Transcripts
NP_055266.2:p.Leu625Phe	CA179797 NM_014451.4:c.1873C>T