Canonical Allele Identifier: PA2829743405
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055266.2:p.Asp21His
CA367189344
NM_014451.4:c.61G>C