Canonical Allele Identifier: PA2828716013
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573243
ClinVar RCV Id: RCV000694867 RCV001830524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364385.1:p.Thr79Pro
CA395985834
NM_001377456.1:c.235A>C