Canonical Allele Identifier: PA2828063479
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2659
ClinVar RCV Id: RCV000002778
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349608.1:p.Gly141Arg
CA252387
NM_001362679.1:c.421G>A
CA367251977
NM_001362679.1:c.421G>C