Canonical Allele Identifier: PA2827421806
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_001334967.1:p.Ala336Val
CA200975
NM_001348038.3:c.1007C>T