Canonical Allele Identifier: PA2827423771
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334971.1:p.Gly39Glu
CA4213908
NM_001348042.3:c.116G>A