Canonical Allele Identifier: PA2827425716
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 286735
ClinVar RCV Id: RCV000392986 RCV001242482
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334974.1:p.Ile518Val
CA4214544
NM_001348045.3:c.1552A>G