Canonical Allele Identifier: PA105691
Gene: BBS7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3015
ClinVar RCV Id: RCV000003151 RCV001091375 RCV001240994 RCV003964791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789794.1:p.His323Arg
CA252533
NM_176824.3:c.968A>G