Canonical Allele Identifier: PA2827425203
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 286735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334973.1:p.Ile483Val
CA4214544
NM_001348044.3:c.1447A>G