Canonical Allele Identifier: PA2573096606
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114091.4:p.Val75Gly
CA253233
NM_031885.5:c.224T>G