Canonical Allele Identifier: PA2827420566
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427492

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334965.1:p.Thr59Lys
CA367190349
NM_001348036.1:c.176C>A