Allele Registry

Canonical Allele Identifier: PA2827421131

Gene: BBS9 HGNC NCBI

ClinVar Allele:

17698

ClinVar RCV:

RCV000002778

ClinVar Variation:

2659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334966.1:p.Gly19Arg	CA252387 NM_001348037.3:c.55G>A CA367251977 NM_001348037.3:c.55G>C