Canonical Allele Identifier: PA2828063856
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 194995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349608.1:p.Thr702Asn
CA241249
NM_001362679.1:c.2105C>A