Allele Registry

Canonical Allele Identifier: PA2827421622

Gene: BBS9 HGNC NCBI

ClinVar RCV:

RCV000002778

ClinVar Variation:

2659

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334967.1:p.Gly50Arg	CA252387 NM_001348038.3:c.148G>A CA367251977 NM_001348038.3:c.148G>C