Canonical Allele Identifier: PA2499303704
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940820.1:p.Leu69Pro
CA4213899
NM_198428.3:c.206T>C