Canonical Allele Identifier: PA2825371907
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1960921
ClinVar RCV Id: RCV002706719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028777.1:p.Asp21His
CA367189344
NM_001033605.2:c.61G>C