Canonical Allele Identifier: PA2827420619
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2659
ClinVar RCV Id: RCV000002778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334965.1:p.Gly141Arg
CA252387
NM_001348036.1:c.421G>A
CA367251977
NM_001348036.1:c.421G>C