Canonical Allele Identifier: PA2827422879
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 194138
ClinVar RCV Id: RCV000174426 RCV000204910 RCV000515021 RCV001095289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334969.1:p.Ala427Val
CA200975
NM_001348040.3:c.1280C>T