Canonical Allele Identifier: PA2827420573
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011247
ClinVar RCV Id: RCV001309012
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334965.1:p.Leu69Pro
CA4213899
NM_001348036.1:c.206T>C