Canonical Allele Identifier: PA2828716055
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 410986
ClinVar RCV Id: RCV000457908 RCV001833591 RCV002523348 RCV002475884 RCV004533200
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Ala120Thr
CA8066063
NM_001377456.1:c.358G>A