Canonical Allele Identifier: PA2573313065
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_940820.1:p.Val87Ile
CA367190662
NM_198428.3:c.259G>A