Canonical Allele Identifier: PA2825371726
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 286735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028776.1:p.Ile605Val
CA4214544
NM_001033604.2:c.1813A>G