Canonical Allele Identifier: PA2829743495
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413469
ClinVar RCV Id: RCV001945030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055266.2:p.Val87Ile
CA367190662
NM_014451.4:c.259G>A