Canonical Allele Identifier: PA2829743388
Gene: BBS9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1963991
ClinVar RCV Id: RCV002716319 RCV003916520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055266.2:p.Arg7Ser
CA4213850
NM_014451.4:c.19C>A