Allele Registry

Canonical Allele Identifier: PA916029769

Gene: BBS9 HGNC NCBI

ClinVar Allele:

17698

ClinVar RCV:

RCV000002778

ClinVar Variation:

2659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334971.1:p.Gly96Arg	CA252387 NM_001348042.3:c.286G>A CA367251977 NM_001348042.3:c.286G>C