Canonical Allele Identifier: PA916050839
Gene: BBS10 HGNC NCBI

Linked Data

ClinVar Variation Id: 658119
ClinVar RCV Id: RCV000814869 RCV001276474 RCV001702720 RCV001816892 RCV002537389 RCV003411796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078961.3:p.Ala296Thr
CA6694269
NM_024685.4:c.886G>A