Canonical Allele Identifier: PA2573291575
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392751
ClinVar RCV Id: RCV001896380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114091.4:p.Asp65Val
CA8066098
NM_031885.5:c.194A>T