Canonical Allele Identifier: PA2827422042
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 242248
ClinVar RCV Id: RCV000514762 RCV001086797 RCV003151001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334967.1:p.Leu688Gln
CA4214668
NM_001348038.3:c.2063T>A