Canonical Allele Identifier: PA2499292535
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1038392
ClinVar RCV Id: RCV001341690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114091.4:p.Val40Gly
CA395986489
NM_031885.5:c.119T>G