Canonical Allele Identifier: PA2827422660
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413469
ClinVar RCV Id: RCV001945030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334969.1:p.Val87Ile
CA367190662
NM_001348040.3:c.259G>A