Canonical Allele Identifier: PA2828063443
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349608.1:p.Gly84Glu
CA4213908
NM_001362679.1:c.251G>A