Allele Registry

Canonical Allele Identifier: PA2827425383

Gene: BBS9 HGNC NCBI

ClinVar RCV:

RCV000002778

ClinVar Variation:

2659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334974.1:p.Gly19Arg	CA252387 NM_001348045.3:c.55G>A CA367251977 NM_001348045.3:c.55G>C