Canonical Allele Identifier: PA2828715993
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516284
ClinVar RCV Id: RCV002040809

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Val52Asp
CA395986278
NM_001377456.1:c.155T>A