Canonical Allele Identifier: PA2825372065
Gene: BBS9 HGNC NCBI
ClinVar RCV:
RCV000256397
ClinVar Variation:
265988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001028777.1:p.Val262Ala
CA10588927
NM_001033605.2:c.785T>C