Canonical Allele Identifier: PA2827425113
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 263119
ClinVar RCV Id: RCV000247367 RCV000368161 RCV000709635 RCV001095136 RCV001706406
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001334973.1:p.Pro359Thr
CA4214392
NM_001348044.3:c.1075C>A