Allele Registry

Canonical Allele Identifier: PA2827421706

Gene: BBS9 HGNC NCBI

ClinVar RCV:

RCV000256397

ClinVar Variation:

265988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001334967.1:p.Val171Ala	CA10588927 NM_001348038.3:c.512T>C