Canonical Allele Identifier: PA2827421622
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_001334967.1:p.Gly50Arg
CA252387
NM_001348038.3:c.148G>A
CA367251977
NM_001348038.3:c.148G>C