Canonical Allele Identifier: PA2573096605
Gene: BBS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 285261
ClinVar RCV Id: RCV000301991 RCV000710724 RCV000989606 RCV001081362 RCV001553955 RCV003888677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_114091.4:p.Ser70Asn
CA8066097
NM_031885.5:c.209G>A