Canonical Allele Identifier: PA2828715982
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038392
ClinVar RCV Id: RCV001341690
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Val40Gly
CA395986489
NM_001377456.1:c.119T>G