Canonical Allele Identifier: PA2827421954
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 286735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334967.1:p.Ile549Val
CA4214544
NM_001348038.3:c.1645A>G