Canonical Allele Identifier: PA2825371366
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028776.1:p.Leu69Pro
CA4213899
NM_001033604.2:c.206T>C