Allele Registry

Canonical Allele Identifier: PA2825371326

Gene: BBS9 HGNC NCBI

ClinVar RCV:

RCV002716319

RCV003916520

ClinVar Variation:

1963991

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028776.1:p.Arg7Ser	CA4213850 NM_001033604.2:c.19C>A