Canonical Allele Identifier: PA2828715990
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2646547
ClinVar RCV Id: RCV003411355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Asn49Asp
CA395986343
NM_001377456.1:c.145A>G