Allele Registry

Canonical Allele Identifier: PA2827423258

Gene: BBS9 HGNC NCBI

ClinVar Allele:

17698

ClinVar RCV:

RCV000002778

ClinVar Variation:

2659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334970.1:p.Gly141Arg	CA252387 NM_001348041.4:c.421G>A CA367251977 NM_001348041.4:c.421G>C