Canonical Allele Identifier: PA2825372065
Gene: BBS9 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028777.1:p.Val262Ala
CA10588927
NM_001033605.2:c.785T>C